rs7626962(T;T)

Now: Benign? Formerly: increased susceptibility to long QT syndrome

Is a	genotype
of	rs7626962
Gene	SCN5A
Chromosome	3
Position	38,579,416
mentioned	by

Magnitude

2

Repute

Bad

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, 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.