V TCF4 | |||
This variant could not be mapped to the genome. Associations 2 Studies 2 |
G TCF4 | |||
Description: transcription factor 4 Associations 496 Studies 327 |
G TCF4-AS2 | |||
Description: TCF4 antisense RNA 2 Associations 2 Studies 2 |
G TCF4-AS1 | |||
Description: TCF4 antisense RNA 1 Associations 16 Studies 14 |
P Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4. | |||
Ellinghaus D et al. 2012 Hepatology PMID:22821403 Associations 2 Studies 1 |
V rs72930774 | |||
Location: 18:55492684 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS2 Associations 1 Studies 1 |
V rs2060889 | |||
Location: 18:55492310 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS2 Associations 1 Studies 1 |
V rs1631486 | |||
Location: 18:55359126 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs9960767 | |||
Location: 18:55487771 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs1261117 | |||
Location: 18:55282426 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs17512836 | |||
Location: 18:55527730 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs1452787 | |||
Location: 18:55539976 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 9 Studies 9 |
V rs17594526 | |||
Location: 18:55391007 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs613872 | |||
Location: 18:55543071 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 38 Studies 38 |
V rs9636107 | |||
Location: 18:55532886 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 13 Studies 13 |
V rs11152369 | |||
Location: 18:55399097 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs78322266 | |||
Location: 18:55396445 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs72926932 | |||
Location: 18:55383415 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 8 Studies 8 |
V rs148138116 | |||
Location: 18:55534249 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs12954356 | |||
Location: 18:55586179 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs11152363 | |||
Location: 18:55389957 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 7 Studies 7 |
V rs7235757 | |||
Location: 18:55400723 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 4 Studies 4 |
V rs11662842 | |||
Location: 18:55257086 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1261093 | |||
Location: 18:55253719 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 7 Studies 7 |
V rs72932713 | |||
Location: 18:55519680 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 7 Studies 7 |
V rs1261070 | |||
Location: 18:55235854 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 5 Studies 5 |
V rs1452789 | |||
Location: 18:55448648 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs7231748 | |||
Location: 18:55441804 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1261114 | |||
Location: 18:55271138 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 4 Studies 4 |
V rs1440476 | |||
Location: 18:55372835 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs7228159 | |||
Location: 18:55437022 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 5 Studies 5 |
V rs12958048 | |||
Location: 18:55434367 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 9 Studies 9 |
V rs12963463 | |||
Location: 18:55431862 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 4 Studies 4 |
V rs599550 | |||
Location: 18:55585157 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 14 Studies 14 |
V rs1262463 | |||
Location: 18:55287190 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs2924322 | |||
Location: 18:55577183 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs28607662 | |||
Location: 18:55563628 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs893946 | |||
Location: 18:55315227 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 4 Studies 4 |
V rs28602385 | |||
Location: 18:55392089 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs2860511 | |||
Location: 18:55416360 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs10503002 | |||
Location: 18:55441971 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs12457157 | |||
Location: 18:55629696 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs13381817 | |||
Location: 18:55230988 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs4801157 | |||
Location: 18:55497462 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 8 Studies 8 |
V rs611439 | |||
Location: 18:55537633 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1452788 | |||
Location: 18:55450073 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs12967143 | |||
Location: 18:55431781 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 10 Studies 10 |
V rs660010 | |||
Location: 18:55643738 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs644279 | |||
Location: 18:55627338 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1011392 | |||
Location: 18:55374672 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs8095770 | |||
Location: 18:55426493 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs17594358 | |||
Location: 18:55383258 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs12607857 | |||
Location: 18:55546095 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs6566169 | |||
Location: 18:55634296 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs2919451 | |||
Location: 18:55417069 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs619466 | |||
Location: 18:55531605 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 10 Studies 10 |
V rs2958184 | |||
Location: 18:55484620 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs17596995 | |||
Location: 18:55499363 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs11659559 | |||
Location: 18:55338703 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs78803556 | |||
Location: 18:55451231 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs17598729 | |||
Location: 18:55584331 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1788030 | |||
Location: 18:55377967 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs149344987 | |||
Location: 18:55381298 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs584564 | |||
Location: 18:55560417 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1660237 | |||
Location: 18:55346716 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs2958162 | |||
Location: 18:55416634 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 4 Studies 4 |
V rs60565673 | |||
Location: 18:55239599 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs8766 | |||
Location: 18:55228300 Cytogenetic region:18q21.2 Most severe consequence: Synonymous variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs2872041 | |||
Location: 18:55397260 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs9950000 | |||
Location: 18:55384938 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs4144686 | |||
Location: 18:55584494 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs17596722 | |||
Location: 18:55486936 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs12607679 | |||
Location: 18:55392517 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs188837888 | |||
Location: 18:55235701 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs624244 | |||
Location: 18:55516165 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs72930755 | |||
Location: 18:55483919 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs72930763 | |||
Location: 18:55487656 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs9320010 | |||
Location: 18:55386666 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs144033370 | |||
Location: 18:55228493 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs150202082 | |||
Location: 18:55360492 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs12458015 | |||
Location: 18:55638504 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1788025 | |||
Location: 18:55381447 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs73487020 | |||
Location: 18:55236369 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs73477270 | |||
Location: 18:55425653 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs66791238 | |||
Location: 18:55563419 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs41396445 | |||
Location: 18:55574906 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs72926982 | |||
Location: 18:55420753 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs76641465 | |||
Location: 18:55319930 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs35371867 | |||
Location: 18:55525796 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs77540208 | |||
Location: 18:55426136 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs8090418 | |||
Location: 18:55288444 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs17594665 | |||
Location: 18:55396488 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs2060886 | |||
Location: 18:55500289 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs590076 | |||
Location: 18:55593501 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs17597926 | |||
Location: 18:55538707 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs12963334 | |||
Location: 18:55431790 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs117652372 | |||
Location: 18:55607167 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs72926972 | |||
Location: 18:55417896 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs2123392 | |||
Location: 18:55547634 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs78245018 | |||
Location: 18:55254431 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1261134 | |||
Location: 18:55264532 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs76888488 | |||
Location: 18:55643770 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs10871582 | |||
Location: 18:55609358 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs79151843 | |||
Location: 18:55264660 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs74441911 | |||
Location: 18:55370474 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs627685 | |||
Location: 18:55518861 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs1630422 | |||
Location: 18:55371253 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs71670792 | |||
Location: 18:55222482 Cytogenetic region:18q21.2 Most severe consequence: 3 prime utr variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1261085 | |||
Location: 18:55222736 Cytogenetic region:18q21.2 Most severe consequence: 3 prime utr variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs41478353 | |||
Location: 18:55230897 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs41515848 | |||
Location: 18:55242588 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs9955026 | |||
Location: 18:55297641 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs2043961 | |||
Location: 18:55375989 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1623427 | |||
Location: 18:55379088 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs1788027 | |||
Location: 18:55275596 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1153637 | |||
Location: 18:55304979 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs12969553 | |||
Location: 18:55434673 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs72928904 | |||
Location: 18:55436137 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs139992005 | |||
Location: 18:55324905 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs72926954 | |||
Location: 18:55402937 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs74914300 | |||
Location: 18:55343117 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1348047 | |||
Location: 18:55382827 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs140282719 | |||
Location: 18:55486362 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs2958163 | |||
Location: 18:55418181 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs56029033 | |||
Location: 18:55483150 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs8098032 | |||
Location: 18:55572071 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs1893431 | |||
Location: 18:55251269 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs12969536 | |||
Location: 18:55434629 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs618869 | |||
Location: 18:55580920 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 3 Studies 3 |
V rs17598416 | |||
Location: 18:55562530 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs72932757 | |||
Location: 18:55587510 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs11412305 | |||
Location: 18:55422101 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs4801154 | |||
Location: 18:55434753 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs76640061 | |||
Location: 18:55225084 Cytogenetic region:18q21.2 Most severe consequence: 3 prime utr variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs17522826 | |||
Location: 18:55403683 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs202020783 | |||
Location: 18:55423807 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs577732976 | |||
Location: 18:55423808 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 6 Studies 6 |
V rs1053076916 | |||
Location: 18:55451663 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs763283047 | |||
Location: 18:55609913 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 1 Studies 1 |
V rs616580 | |||
Location: 18:55616878 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4 Associations 2 Studies 2 |
V rs2924328 | |||
Location: 18:55466509 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS1 Associations 2 Studies 2 |
V rs2924321 | |||
Location: 18:55458204 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS1 Associations 1 Studies 1 |
V rs896686 | |||
Location: 18:55455800 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS1 Associations 1 Studies 1 |
V rs2958182 | |||
Location: 18:55481790 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS1 Associations 1 Studies 1 |
V rs2958183 | |||
Location: 18:55482845 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS1 Associations 5 Studies 5 |
V rs144933108 | |||
Location: 18:55459689 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS1 Associations 1 Studies 1 |
V rs2924329 | |||
Location: 18:55468663 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS1 Associations 3 Studies 3 |
V rs17596267 | |||
Location: 18:55474306 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS1 Associations 1 Studies 1 |
V rs12606995 | |||
Location: 18:55454345 Cytogenetic region:18q21.2 Most severe consequence: Intron variant Mapped gene(s): TCF4,TCF4-AS1 Associations 1 Studies 1 |
V rs9951150 | |||
Location: 18:55153893 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 3 Studies 3 |
V rs1970671 | |||
Location: 18:55195877 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs12458596 | |||
Location: 18:55743681 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 2 Studies 2 |
V rs1262465 | |||
Location: 18:55190501 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 2 Studies 2 |
V rs784257 | |||
Location: 18:55729968 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 14 Studies 14 |
V rs28758902 | |||
Location: 18:55740956 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 5 Studies 5 |
V rs1031831 | |||
Location: 18:55680027 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 4 Studies 4 |
V rs784256 | |||
Location: 18:55731395 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 5 Studies 5 |
V rs4800995 | |||
Location: 18:55748146 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 2 Studies 2 |
V rs11659764 | |||
Location: 18:55668281 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 40 Studies 40 |
V rs1642294 | |||
Location: 18:55707682 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 2 Studies 2 |
V rs1011339 | |||
Location: 18:55153832 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs4801146 | |||
Location: 18:55173694 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 2 Studies 2 |
V rs1125313 | |||
Location: 18:55192030 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs4801147 | |||
Location: 18:55205475 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs17536 | |||
Location: 18:55776658 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs784242 | |||
Location: 18:55769972 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs72932563 | |||
Location: 18:55770428 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 2 Studies 2 |
V rs1942262 | |||
Location: 18:55206086 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 4 Studies 4 |
V rs2051293 | |||
Location: 18:55150778 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 2 Studies 2 |
V rs9957512 | |||
Location: 18:55207430 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 2 Studies 2 |
V rs4800998 | |||
Location: 18:55762424 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 2 Studies 2 |
V rs784219 | |||
Location: 18:55684253 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs1261078 | |||
Location: 18:55199560 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 2 Studies 2 |
V rs9960987 | |||
Location: 18:55763160 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs57820851 | |||
Location: 18:55746335 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 4 Studies 4 |
V rs11665450 | |||
Location: 18:55177535 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs8086468 | |||
Location: 18:55189482 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs12457071 | |||
Location: 18:55692242 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs12456049 | |||
Location: 18:55759211 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs76235101 | |||
Location: 18:55169327 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs899104 | |||
Location: 18:55721830 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs75828199 | |||
Location: 18:55679508 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs113682423 | |||
Location: 18:55676990 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs77882218 | |||
Location: 18:55747832 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs61043970 | |||
Location: 18:55214391 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 5 Studies 5 |
V rs77528088 | |||
Location: 18:55192126 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs2226740 | |||
Location: 18:55151815 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 2 Studies 2 |
V rs11152291 | |||
Location: 18:55221836 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs1111935 | |||
Location: 18:55207493 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs34704381 | |||
Location: 18:55708446 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs76124729 | |||
Location: 18:55167042 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs77262239 | |||
Location: 18:55220713 Cytogenetic region:18q21.2 Most severe consequence: Regulatory region variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs1942893 | |||
Location: 18:55150935 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 2 Studies 2 |
V rs36059932 | |||
Location: 18:55753345 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs1788014 | |||
Location: 18:55219205 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs4800994 | |||
Location: 18:55736619 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs4800996 | |||
Location: 18:55757127 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs8098857 | |||
Location: 18:55207717 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs375200965 | |||
Location: 18:55694077 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs17527878 | |||
Location: 18:55737755 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 2 Studies 2 |
V rs1261094 | |||
Location: 18:55200861 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs187698281 | |||
Location: 18:55220120 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 2 Studies 2 |
V rs7243387 | |||
Location: 18:55215419 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 2 Studies 2 |
V rs7241526 | |||
Location: 18:55203534 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs6567200 | |||
Location: 18:55203606 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 2 Studies 2 |
V rs79123839 | |||
Location: 18:55203453 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs1942569 | |||
Location: 18:55179494 Cytogenetic region:18q21.2 Most severe consequence: Regulatory region variant Mapped gene(s): TCF4,RNA5SP459 Associations 1 Studies 1 |
V rs17089932 | |||
Location: 18:55761116 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |
V rs75802037 (rs776081653) | |||
Location: 18:55684309 Cytogenetic region:18q21.2 Most severe consequence: Intergenic variant Mapped gene(s): TCF4,LINC01415 Associations 1 Studies 1 |