Disease: LONG QT SYNDROME 1/2, DIGENIC (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs120074196
rs120074196
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C3277700
Disease:
LONG QT SYNDROME 1/2, DIGENIC (disorder) 		C 0.700 CausalMutation CLINVAR
dbSNP: rs12720459
rs12720459
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C3277700
Disease:
LONG QT SYNDROME 1/2, DIGENIC (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs397508116
rs397508116
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C3277700
Disease:
LONG QT SYNDROME 1/2, DIGENIC (disorder) 		C 0.700 CausalMutation CLINVAR