V rs231362 | |||
Location: 11:2670241 Cytogenetic region:11p15.5 Most severe consequence: Intron variant Mapped gene(s): KCNQ1OT1,KCNQ1 Associations 9 Studies 8 |
G KCNQ1OT1 | |||
Description: KCNQ1 opposite strand/antisense transcript 1 Associations 66 Studies 51 |
G KCNQ1 | |||
Description: potassium voltage-gated channel subfamily Q member 1 Associations 604 Studies 272 |