Disease: Long QT Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060500661
rs1060500661
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
CUI: C0023976
Disease:
Long QT Syndrome 		A 0.700 CausalMutation CLINVAR