Short Qt Syndrome Type 1
Other
58 variants
3 genes
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to see your personal risk score for Short Qt Syndrome Type 1.
Associated Genes (3)
KCNH2
KCNQ1
KCNJ2
Associated Variants (58)
RSID
Gene
Risk Allele
Odds Ratio
Evidence
RS906562788
KCNH2
—
—
strong
RS794728504
KCNH2
—
—
strong
RS748706373
KCNH2
—
—
strong
RS794728399
KCNH2
—
—
strong
RS765427343
KCNH2
—
—
strong
RS794728382
KCNH2
—
—
strong
RS794728480
KCNH2
—
—
strong
RS370637245
KCNH2
—
—
strong
RS562875924
KCNH2
—
—
strong
RS551056698
KCNH2
—
—
strong
RS569452580
KCNH2
—
—
strong
RS778879572
KCNH2
—
—
strong
RS972201049
KCNH2
—
—
strong
RS373394254
KCNH2
—
—
strong
RS367570298
KCNH2
—
—
strong
RS376308069
KCNH2
—
—
strong
RS762510312
KCNH2
—
—
strong
RS1554423871
KCNH2
—
—
strong
RS372023163
KCNH2
—
—
strong
RS374912424
KCNH2
—
—
strong
RS768652751
KCNH2
—
—
strong
RS1350217087
KCNH2
—
—
strong
RS758978727
KCNH2
—
—
strong
RS778276270
KCNH2
—
—
strong
RS2116964263
KCNH2
—
—
strong
RS199472999
KCNH2
—
—
strong
RS121912507
KCNH2
—
—
strong
RS104894021
KCNH2
—
—
strong
RS121912514
KCNH2
—
—
strong
RS121912515
KCNH2
—
—
strong
RS199473457
KCNQ1
—
—
strong
RS199472837
KCNH2
—
—
strong
RS199473490
KCNH2
—
—
strong
RS199472910
KCNH2
—
—
strong
RS199473428
KCNH2
—
—
strong
RS199473524
KCNH2
—
—
strong
RS199472957
KCNH2
—
—
strong
RS199473422
KCNH2
—
—
strong
RS121912504
KCNH2
—
—
strong
RS199472851
KCNH2
—
—
strong
RS143512106
KCNH2
—
—
strong
RS199473669
KCNH2
—
—
strong
RS199473435
KCNH2
—
—
strong
RS76420733
KCNH2
—
—
strong
RS199473439
KCNH2
—
—
strong
RS199473009
KCNH2
—
—
strong
RS36210422
KCNH2
—
—
strong
RS150817714
KCNH2
—
—
strong
RS199473377
KCNJ2
—
—
strong
RS751559990
KCNH2
—
—
strong
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