rs76173977(C;T)

Carrier of a Tay-Sachs mutation

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs76173977(C;T)
Gene
HEXA

Other genotypes of rs76173977

  1. C;CGoodcommon in clinvarTypical · 0.0
  2. T;TMost notableBadTay-Sachs diseaseVery important · 8.8

All about rs76173977

Notes

From SNPedia

Unaffected in absence of a second HEXA gene mutation; see discussion at Tay-Sachs disease.

Source and license

Adapted from rs76173977(C;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.