Gene: SCN5A ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199473603
rs199473603
SCN5A
A 0.710 GeneticVariation CLINVAR

dbSNP: rs749697698
rs749697698
SCN5A
G 0.700 GeneticVariation CLINVAR Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. 19716085

2009
dbSNP: rs749697698
rs749697698
SCN5A
G 0.700 GeneticVariation CLINVAR [Novel SCN5A gene mutations associated with Brugada syndrome: V95I, A1649V and delF1617]. 17081365

2006
dbSNP: rs749697698
rs749697698
SCN5A
G 0.700 GeneticVariation CLINVAR Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. 10973849

2000
dbSNP: rs199473124
rs199473124
SCN5A
T 0.700 GeneticVariation CLINVAR

dbSNP: rs72549410
rs72549410
SCN5A
T 0.700 CausalMutation CLINVAR