Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201460753
rs201460753
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
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