rs7626962(T;T)

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

Magnitude
2.0Worth knowing
Repute
Bad
Frequency
0%Average of 4 populations
On SNPedia
rs7626962(T;T)
Gene
SCN5A

Frequency

Share of people with T;T in each HapMap population.

  • European ancestry (Utah)0%
  • Yoruba (Nigeria)0%
  • African ancestry (Southwest US)0%
  • Luhya (Kenya)0%

Other genotypes of rs7626962

  1. G;GGoodcommon in clinvarTypical · 0.093% of people
  2. G;TMost notableBadNow: Benign? Formerly: increased susceptibility to long QT syndromeWorth knowing · 2.07% of people

All about rs7626962

Notes

From SNPedia

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.

Source and license

Adapted from rs7626962(T;T) on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.