Disease: SHORT QT SYNDROME 2 (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs120074193
rs120074193
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C1865019
Disease:
SHORT QT SYNDROME 2 (disorder) 		A 0.700 CausalMutation CLINVAR