Short Qt Syndrome Type 2

Other 94 variants 1 gene

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Associated Genes (1)
Associated Variants (94)
RSID Gene Risk Allele Odds Ratio Evidence
RS774101297 KCNQ1 strong
RS1554958045 KCNQ1 strong
RS1057519584 KCNQ1 strong
RS370023636 KCNQ1 strong
RS146350010 KCNQ1 strong
RS1001293702 KCNQ1 strong
RS1435990592 KCNQ1 strong
RS368011737 KCNQ1 strong
RS1564820372 KCNQ1 strong
RS1263583359 KCNQ1 strong
RS775362401 KCNQ1 strong
RS747704276 KCNQ1 strong
RS1590081467 KCNQ1 strong
RS181226788 KCNQ1 strong
RS1848319199 KCNQ1 strong
RS771815387 KCNQ1 strong
RS200796314 KCNQ1 strong
RS1848365236 KCNQ1 strong
RS747187696 KCNQ1 strong
RS753256800 KCNQ1 strong
RS780676796 KCNQ1 strong
RS763478809 KCNQ1 strong
RS2133730742 KCNQ1 strong
RS528825731 KCNQ1 strong
RS2494325585 KCNQ1 strong
RS750409379 KCNQ1 strong
RS139042529 KCNQ1 strong
RS199472696 KCNQ1 strong
RS371488379 KCNQ1 strong
RS186188610 KCNQ1 strong
RS201698592 KCNQ1 strong
RS532941548 KCNQ1 strong
RS148121889 KCNQ1 strong
RS147091980 KCNQ1 strong
RS727504769 KCNQ1 strong
RS76735093 KCNQ1 strong
RS149089817 KCNQ1 strong
RS370676650 KCNQ1 strong
RS397508097 KCNQ1 strong
RS11601907 KCNQ1 strong
RS144615901 KCNQ1 strong
RS112113213 KCNQ1 strong
RS886048160 KCNQ1 strong
RS770840921 KCNQ1 strong
RS189162344 KCNQ1 strong
RS186055804 KCNQ1 strong
RS727505084 KCNQ1 strong
RS774059974 KCNQ1 strong
RS201682200 KCNQ1 strong
RS139633955 KCNQ1 strong
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