rs121907970(C;C)

Miscall by Ancestry; actually represents the common/benign genotype

Magnitude
0.0Typical
Repute
Good
On SNPedia
rs121907970(G;G)Minus strand
Gene
HEXA

Other genotypes of rs121907970

  1. G;GGoodcommon in clinvarTypical · 0.0
  2. A;GMost notableNot ratedCarrier of a Tay-Sachs pseudodeficiency alleleWorth knowing · 2.0

All about rs121907970

Notes

From SNPedia

Error by Ancestry; this should be the (C;C) common/benign genotype.

Source and license

Adapted from rs121907970(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.