Disease: Atrial Fibrillation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72550247
rs72550247
Entrez Id: 3249;6324
Gene Symbol: HPN;SCN1B
HPN;SCN1B
CUI: C0004238
Disease:
Atrial Fibrillation 		0.010 GeneticVariation BEFREE We identified 2 nonsynonymous variants in SCN1B (resulting in R85H, D153N) and 2 in SCN2B (R28Q, R28W) in patients with AF. 19808477 2009