Disease: LONG QT SYNDROME 3/6, DIGENIC Disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137854600
rs137854600
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C3276241
Disease:
LONG QT SYNDROME 3/6, DIGENIC Disorder 		T 0.700 CausalMutation CLINVAR