Have questions? Visit https://www.reddit.com/r/SNPedia

rs7626962(T;T)

From SNPedia

increased susceptibility to long QT syndrome
Is agenotype
ofrs7626962
GeneSCN5A
Chromosome3
Position38,579,416
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 increased susceptibility to long QT syndrome
(T;T) 4 increased susceptibility to long QT syndrome

The rs7626962(T) allele has been associated with higher risk of syncope, ventricular arrhythmia, and ventricular fibrillation, and in one study, this (T;T) genotype was reported to be at 24 fold higher risk for sudden infant death syndrome compared to those without any T alleles.