Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554424083
rs1554424083
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
CUI: C0023976
Disease:
Long QT Syndrome
GCCGAC 0.700 CausalMutation CLINVAR