Congenital Long Qt Syndrome
Other
455 variants
6 genes
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to see your personal risk score for Congenital Long Qt Syndrome.
Associated Genes (6)
SCN5A
KCNJ2
KCNE1
KCNH2
KCNQ1
KCNE2
Associated Variants (455)
RSID
Gene
Risk Allele
Odds Ratio
Evidence
RS137854617
SCN5A
—
—
strong
RS104894581
KCNJ2
—
—
strong
RS104894582
KCNJ2
—
—
strong
RS104894583
KCNJ2
—
—
strong
RS104894585
KCNJ2
—
—
strong
RS28937316
SCN5A
—
—
strong
RS28937317
SCN5A
—
—
strong
RS137854614
SCN5A
—
—
strong
RS137854600
SCN5A
—
—
strong
RS137854601
SCN5A
—
—
strong
RS137854609
SCN5A
—
—
strong
RS137854611
SCN5A
—
—
strong
RS137854612
SCN5A
—
—
strong
RS104894580
KCNJ2
—
—
strong
RS137854619
SCN5A
—
—
strong
RS28933384
KCNE1
—
—
strong
RS74315445
KCNE1
—
—
strong
RS74315446
KCNE1
—
—
strong
RS1805128
KCNE1
—
—
strong
RS121912504
KCNH2
—
—
strong
RS121912505
KCNH2
—
—
strong
RS28928904
KCNH2
—
—
strong
RS121912506
KCNH2
—
—
strong
RS121912507
KCNH2
—
—
strong
RS2496741859
KCNQ1
—
—
strong
RS1800171
KCNQ1
—
—
strong
RS120074181
KCNQ1
—
—
strong
RS120074182
KCNQ1
—
—
strong
RS120074178
KCNQ1
—
—
strong
RS120074179
KCNQ1
—
—
strong
RS120074180
KCNQ1
—
—
strong
RS12720459
KCNQ1
—
—
strong
RS120074183
KCNQ1
—
—
strong
RS120074184
KCNQ1
—
—
strong
RS120074185
KCNQ1
—
—
strong
RS120074186
KCNQ1
—
—
strong
RS17215500
KCNQ1
—
—
strong
RS120074188
KCNQ1
—
—
strong
RS120074177
KCNQ1
—
—
strong
RS120074189
KCNQ1
—
—
strong
RS120074190
KCNQ1
—
—
strong
RS120074191
KCNQ1
—
—
strong
RS17221854
KCNQ1
—
—
strong
RS120074193
KCNQ1
—
—
strong
RS120074194
KCNQ1
—
—
strong
RS120074196
KCNQ1
—
—
strong
RS74315447
KCNE2
—
—
strong
RS16991654
KCNE2
—
—
strong
RS104894575
KCNJ2
—
—
strong
RS104894579
KCNJ2
—
—
strong
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