G BBS9 | |||
Description: Bardet-Biedl syndrome 9 Associations 83 Studies 62 |
P A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9. | |||
Justice CM et al. 2012 Nat Genet PMID:23160099 Associations 2 Studies 1 |
V rs17169807 | |||
Location: 7:33141626 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs17170316 | |||
Location: 7:33633653 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs10262453 | |||
Location: 7:33216427 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs10262995 | |||
Location: 7:33510429 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs4720118 | |||
Location: 7:33429629 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs3815652 | |||
Location: 7:33873792 Cytogenetic region:7p14.3 Most severe consequence: Regulatory region variant Mapped gene(s): BBS9 Associations 2 Studies 2 |
V rs202162020 | |||
Location: 7:33466057 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs75178228 | |||
Location: 7:33829191 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs78717017 | |||
Location: 7:33824955 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs111736039 | |||
Location: 7:33828710 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs113407698 | |||
Location: 7:33832978 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs77255239 | |||
Location: 7:33838119 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs77998448 | |||
Location: 7:33839927 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs771362288 | |||
Location: 7:33747371 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs1362227 | |||
Location: 7:33472019 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 3 Studies 3 |
V rs17170187 | |||
Location: 7:33328851 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs10232036 | |||
Location: 7:33212340 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs12701320 | |||
Location: 7:33710529 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs117742456 | |||
Location: 7:33455612 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs79995619 | |||
Location: 7:33501518 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs2392165 | |||
Location: 7:33120302 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs17170333 | |||
Location: 7:33662379 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs6462481 | |||
Location: 7:33471004 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 2 Studies 2 |
V rs12701336 | |||
Location: 7:33874148 Cytogenetic region:7p14.3 Most severe consequence: Regulatory region variant Mapped gene(s): BBS9 Associations 3 Studies 1 |
V rs11773485 | |||
Location: 7:33669340 Cytogenetic region:7p14.3 Most severe consequence: Regulatory region variant Mapped gene(s): BBS9 Associations 2 Studies 1 |
V rs7779722 | |||
Location: 7:33559009 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs7785398 | |||
Location: 7:33826129 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs62451225 | |||
Location: 7:33501113 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs4723276 | |||
Location: 7:33220181 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs9768604 | |||
Location: 7:33222578 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs10225173 | |||
Location: 7:33244683 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 6 Studies 6 |
V rs10228486 | |||
Location: 7:33214968 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 2 Studies 2 |
V rs6947352 | |||
Location: 7:33222938 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs4723263 | |||
Location: 7:33155214 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs10250448 | |||
Location: 7:33449611 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs6946608 | |||
Location: 7:33284492 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 3 Studies 3 |
V rs12671896 | |||
Location: 7:33786977 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs1362928 | |||
Location: 7:33794710 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs4723335 | |||
Location: 7:33808280 Cytogenetic region:7p14.3 Most severe consequence: Regulatory region variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs12154346 | |||
Location: 7:33504026 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs1451018 | |||
Location: 7:33561327 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 3 Studies 3 |
V rs78323097 | |||
Location: 7:33518291 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs12534242 | |||
Location: 7:33224538 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 2 Studies 2 |
V rs7785463 | |||
Location: 7:33229477 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs1919786 | |||
Location: 7:33127189 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs1894810 | |||
Location: 7:33468240 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs3757502 | |||
Location: 7:33723971 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs315853 | |||
Location: 7:33876532 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs1420149 | |||
Location: 7:33133547 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs4723334 | |||
Location: 7:33799502 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs12531851 | |||
Location: 7:33776832 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs16879245 | |||
Location: 7:33764873 Cytogenetic region:7p14.3 Most severe consequence: Regulatory region variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs13220931 | |||
Location: 7:33750963 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs117363837 | |||
Location: 7:33119792 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs78294974 | |||
Location: 7:33144410 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs2232125 | |||
Location: 7:33728099 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 2 Studies 2 |
V rs148673350 | |||
Location: 7:33219926 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs1544557 | |||
Location: 7:33469318 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs1362228 | |||
Location: 7:33465686 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs552018321 | |||
Location: 7:33118940 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs538292275 | |||
Location: 7:33118939 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs10246905 | |||
Location: 7:33744692 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs34192176 | |||
Location: 7:33599362 Cytogenetic region:7p14.3 Most severe consequence: Intron variant Mapped gene(s): BBS9 Associations 1 Studies 1 |
V rs111739575 | |||
Location: 7:33797968 Cytogenetic region:7p14.3 Most severe consequence: Intergenic variant Mapped gene(s): BBS9 Associations 1 Studies 1 |