Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16969925
rs16969925
SCN1B
0.800 GeneticVariation UNIPROT

dbSNP: rs16969925
rs16969925
SCN1B
A 0.800 CausalMutation CLINVAR

dbSNP: rs72550247
rs72550247
HPN ; SCN1B
0.700 GeneticVariation UNIPROT Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477

2009
dbSNP: rs104894718
rs104894718
SCN1B
G 0.700 GeneticVariation CLINVAR

dbSNP: rs104894718
rs104894718
SCN1B
G 0.700 CausalMutation CLINVAR