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rs7626962(G;T)

From SNPedia

Now: Benign? Formerly: increased susceptibility to long QT syndrome
Is agenotype
ofrs7626962
GeneSCN5A
Chromosome3
Position38,579,416
mentionedby
Magnitude2
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 2 Now: Benign? Formerly: increased susceptibility to long QT syndrome
(T;T) 2 Now: Benign? Formerly: increased susceptibility to long QT syndrome

See discussion at rs7626962; the rs7626962(T) allele was formerly associated with higher risk of syncope, ventricular arrhythmia, and ventricular fibrillation.