Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894718
rs104894718
Entrez Id: 6324
Gene Symbol: SCN1B
SCN1B
CUI: C3809311
Disease:
ATRIAL FIBRILLATION, FAMILIAL, 13
G 0.700 GeneticVariation CLINVAR
dbSNP: rs104894718
rs104894718
Entrez Id: 6324
Gene Symbol: SCN1B
SCN1B
CUI: C3809311
Disease:
ATRIAL FIBRILLATION, FAMILIAL, 13
G 0.700 CausalMutation CLINVAR