rs7626962(G;G)

Common in clinvar

Magnitude
0.0Typical
Repute
Good
Frequency
93%Average of 4 populations
On SNPedia
rs7626962(G;G)
Gene
SCN5A

Frequency

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

  • European ancestry (Utah)99%
  • Luhya (Kenya)94%
  • African ancestry (Southwest US)91%
  • Yoruba (Nigeria)86%

Other genotypes of rs7626962

  1. G;TMost notableBadNow: Benign? Formerly: increased susceptibility to long QT syndromeWorth knowing · 2.07% of people
  2. T;TBadNow: Benign? Formerly: increased susceptibility to long QT syndromeWorth knowing · 2.00% of people

All about rs7626962

Source and license

Adapted from rs7626962(G;G) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.