G SETBP1 | |||
Description: SET binding protein 1 Associations 187 Studies 141 |
G SETBP1-DT | |||
Description: SETBP1 divergent transcript Associations 30 Studies 30 |
V rs4890489 | |||
Location: 18:44851279 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs17783459 | |||
Location: 18:44749111 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs10853525 | |||
Location: 18:44856687 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs991014 | |||
Location: 18:44859921 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 3 Studies 2 |
V rs9949121 | |||
Location: 18:44726919 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs17782904 | |||
Location: 18:44733745 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs4084232 | |||
Location: 18:44719084 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs6507583 | |||
Location: 18:44819625 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 4 Studies 4 |
V rs9954058 | |||
Location: 18:44831838 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs62092684 | |||
Location: 18:44905484 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs7233512 | |||
Location: 18:45015111 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 4 Studies 4 |
V rs34233878 | |||
Location: 18:45014315 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs684329 | |||
Location: 18:44862174 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs28550327 | |||
Location: 18:44724135 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs16978162 | |||
Location: 18:44776250 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs11082416 | |||
Location: 18:44969513 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs1276250 | |||
Location: 18:44860573 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 4 Studies 4 |
V rs2032231 | |||
Location: 18:45062200 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs663651 | |||
Location: 18:44876688 Cytogenetic region:18q12.3 Most severe consequence: Missense variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs16978240 | |||
Location: 18:44969292 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs11874040 | |||
Location: 18:45016031 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 5 Studies 5 |
V rs11661654 | |||
Location: 18:44861478 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 4 Studies 4 |
V rs9945779 | |||
Location: 18:44813855 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs16978169 | |||
Location: 18:44782004 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs9807656 | |||
Location: 18:44766991 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs11664848 | |||
Location: 18:44995696 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs1126225 | |||
Location: 18:44844629 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 7 Studies 1 |
V rs117763335 | |||
Location: 18:44680383 Cytogenetic region:18q12.3 Most severe consequence: 5 prime utr variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs4890490 | |||
Location: 18:44857303 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs9967367 | |||
Location: 18:45026126 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 7 Studies 7 |
V rs10539959 | |||
Location: 18:44711359 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs614797 | |||
Location: 18:44857349 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 3 Studies 3 |
V rs202209118 | |||
Location: 18:44781459 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs11876680 | |||
Location: 18:44781507 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs7230240 | |||
Location: 18:45018013 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs2852772 | |||
Location: 18:44682904 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs12373476 | |||
Location: 18:44759137 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs586125 | |||
Location: 18:44859114 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs371202693 | |||
Location: 18:44802519 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs3744824 | |||
Location: 18:44951272 Cytogenetic region:18q12.3 Most severe consequence: Missense variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs11082406 | |||
Location: 18:44765621 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs79926430 | |||
Location: 18:44772488 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs12971067 | |||
Location: 18:45026059 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs2615000 | |||
Location: 18:44712119 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs12962548 | |||
Location: 18:45019202 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs200931857 | |||
Location: 18:44701045 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs8096662 | |||
Location: 18:44953165 Cytogenetic region:18q12.3 Most severe consequence: Synonymous variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs954018 | |||
Location: 18:45018498 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs2852780 | |||
Location: 18:44697023 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 3 Studies 3 |
V rs11082403 | |||
Location: 18:44737825 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 2 Studies 2 |
V rs12604120 | |||
Location: 18:44936293 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs17795516 | |||
Location: 18:45018827 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs716152 | |||
Location: 18:45025907 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs114083253 | |||
Location: 18:44842949 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs34038580 | |||
Location: 18:44839474 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs187572799 | |||
Location: 18:44715322 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs9967532 | |||
Location: 18:44728675 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs75551055 | |||
Location: 18:45005576 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs16978179 | |||
Location: 18:44806588 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 3 Studies 3 |
V rs11876574 | |||
Location: 18:45015879 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs669738 | |||
Location: 18:44885992 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs7236215 | |||
Location: 18:44758539 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs11874246 | |||
Location: 18:45016824 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs116997934 | |||
Location: 18:45018456 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs683461 | |||
Location: 18:44873861 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs58306981 | |||
Location: 18:44747009 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs998124 | |||
Location: 18:45145697 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs269985 | |||
Location: 18:45206032 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 2 Studies 2 |
V rs8095987 | |||
Location: 18:45157319 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs62090515 | |||
Location: 18:45091671 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 3 Studies 3 |
V rs11876432 | |||
Location: 18:45089460 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs1450807 | |||
Location: 18:45123701 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 2 Studies 2 |
V rs11082430 | |||
Location: 18:45172412 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs17739187 | |||
Location: 18:45169491 Cytogenetic region:18q12.3 Most severe consequence: Regulatory region variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs12326164 | |||
Location: 18:45096963 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs12959213 | |||
Location: 18:45189055 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs72898831 | |||
Location: 18:45078678 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 5 Studies 5 |
V rs11877152 | |||
Location: 18:45174503 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 3 Studies 3 |
V rs10438961 | |||
Location: 18:45199142 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 3 Studies 3 |
V rs6507603 | |||
Location: 18:45168215 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs2614993 | |||
Location: 18:44677335 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT Associations 1 Studies 1 |
V rs10163551 | |||
Location: 18:45197099 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 3 Studies 3 |
V rs269972 | |||
Location: 18:45197513 Cytogenetic region:18q12.3 Most severe consequence: Regulatory region variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs35053058 (rs533213634) | |||
Location: 18:45053766 Cytogenetic region:18q12.3 Most severe consequence: Intron variant Mapped gene(s): SETBP1 Associations 1 Studies 1 |
V rs72902636 | |||
Location: 18:45158997 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs1026186 | |||
Location: 18:45161445 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs72902641 | |||
Location: 18:45159544 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 2 Studies 2 |
V rs9807214 | |||
Location: 18:45202987 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 4 Studies 4 |
V rs921385 | |||
Location: 18:45204084 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs35398628 | |||
Location: 18:45089927 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs1037320 | |||
Location: 18:45123943 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs269967 | |||
Location: 18:45196470 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs11663494 | |||
Location: 18:45159196 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 2 Studies 2 |
V rs17811812 | |||
Location: 18:45160038 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 2 Studies 2 |
V rs17740207 | |||
Location: 18:45200046 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs11873164 | |||
Location: 18:45079957 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 2 Studies 2 |
V rs7227395 | |||
Location: 18:45075623 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs4890521 | |||
Location: 18:45133252 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs16978286 | |||
Location: 18:45162021 Cytogenetic region:18q12.3 Most severe consequence: Tf binding site variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs117770211 | |||
Location: 18:45078216 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs11877664 | |||
Location: 18:45166494 Cytogenetic region:18q12.3 Most severe consequence: Tf binding site variant Mapped gene(s): SETBP1,SLC14A2 Associations 3 Studies 3 |
V rs17740231 | |||
Location: 18:45201918 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs9973048 | |||
Location: 18:45212938 Cytogenetic region:18q12.3 Most severe consequence: Regulatory region variant Mapped gene(s): SETBP1,SLC14A2 Associations 2 Studies 2 |
V rs11082431 | |||
Location: 18:45201409 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 4 Studies 4 |
V rs141363425 | |||
Location: 18:45152207 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs117206739 | |||
Location: 18:45172745 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs117913008 | |||
Location: 18:45134375 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs117040084 | |||
Location: 18:45078489 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs75497489 | |||
Location: 18:45180235 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs72902690 | |||
Location: 18:45186271 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs56212930 | |||
Location: 18:45194685 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs535560294 | |||
Location: 18:45198216 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1,SLC14A2 Associations 1 Studies 1 |
V rs117867915 | |||
Location: 18:44630078 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 1 Studies 1 |
V rs138775024 | |||
Location: 18:44672443 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 1 Studies 1 |
V rs4890487 | |||
Location: 18:44650207 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 3 Studies 3 |
V rs78306018 | |||
Location: 18:44615220 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 1 Studies 1 |
V rs35726977 (rs145682704) | |||
Location: 18:44604215 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 1 Studies 1 |
V rs1849209 | |||
Location: 18:44581678 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 5 Studies 5 |
V rs7232604 | |||
Location: 18:44608318 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 2 Studies 2 |
V rs34039016 | |||
Location: 18:44622962 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 2 Studies 2 |
V rs2852747 | |||
Location: 18:44650492 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 1 Studies 1 |
V rs2852770 | |||
Location: 18:44666476 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 1 Studies 1 |
V rs11661473 | |||
Location: 18:44597158 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 2 Studies 2 |
V rs56407827 | |||
Location: 18:44599854 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 2 Studies 2 |
V rs16978104 | |||
Location: 18:44584858 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 1 Studies 1 |
V rs117212304 | |||
Location: 18:44641379 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 1 Studies 1 |
V rs35033610 | |||
Location: 18:44606687 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 1 Studies 1 |
V rs1563992 | |||
Location: 18:44665801 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 3 Studies 3 |
V rs8087685 | |||
Location: 18:44629631 Cytogenetic region:18q12.3 Most severe consequence: Intergenic variant Mapped gene(s): SETBP1-DT,LINC01478 Associations 1 Studies 1 |