G STARD10 | |||
Description: StAR related lipid transfer domain containing 10 Associations 44 Studies 44 |
V rs77106637 | |||
Location: 11:72767275 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 2 Studies 2 |
V rs56133113 | |||
Location: 11:72790175 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 3 Studies 3 |
V rs555655470 | |||
Location: 11:72775621 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 3 Studies 3 |
V rs1277060 | |||
Location: 11:72762217 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 3 Studies 3 |
V rs519790 | |||
Location: 11:72793096 Cytogenetic region:11q13.4 Most severe consequence: 5 prime utr variant Mapped gene(s): STARD10,ARAP1 Associations 4 Studies 4 |
V rs7121935 | |||
Location: 11:72785103 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 1 Studies 1 |
V rs663015 | |||
Location: 11:72787990 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 3 Studies 3 |
V rs4944804 | |||
Location: 11:72809485 Cytogenetic region:11q13.4 Most severe consequence: Intergenic variant Mapped gene(s): ATG16L2,STARD10 Associations 1 Studies 1 |
V rs11398692 | |||
Location: 11:72790363 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 2 Studies 2 |
V rs481206 | |||
Location: 11:72786417 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 3 Studies 3 |
V rs3862791 | |||
Location: 11:72789957 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 1 Studies 1 |
V rs35916673 | |||
Location: 11:72798293 Cytogenetic region:11q13.4 Most severe consequence: Intergenic variant Mapped gene(s): ATG16L2,STARD10 Associations 1 Studies 1 |
V rs71062788 | |||
Location: 11:72796214 Cytogenetic region:11q13.4 Most severe consequence: Intergenic variant Mapped gene(s): ATG16L2,STARD10 Associations 1 Studies 1 |
V rs140130268 | |||
Location: 11:72759871 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 3 Studies 3 |
V rs11235598 | |||
Location: 11:72810242 Cytogenetic region:11q13.4 Most severe consequence: Intergenic variant Mapped gene(s): ATG16L2,STARD10 Associations 1 Studies 1 |
V rs660043 | |||
Location: 11:72767202 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 1 Studies 1 |
V rs10898880 | |||
Location: 11:72814066 Cytogenetic region:11q13.4 Most severe consequence: Regulatory region variant Mapped gene(s): ATG16L2,STARD10 Associations 1 Studies 1 |
V rs4944796 | |||
Location: 11:72787955 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 1 Studies 1 |
V rs72964900 | |||
Location: 11:72789879 Cytogenetic region:11q13.4 Most severe consequence: Intron variant Mapped gene(s): STARD10,ARAP1 Associations 6 Studies 6 |
V rs4459332 | |||
Location: 11:72797222 Cytogenetic region:11q13.4 Most severe consequence: Intergenic variant Mapped gene(s): ATG16L2,STARD10 Associations 3 Studies 3 |