rs121965048

A SNP in the OAT gene on chromosome 10. Its most notable genotype is T;T: Likely miscall if from Ancestry or Genes for Good; otherwise, possible mutation

Gene
OAT
Location
Chr 10124,412,010 (GRCh38)
Highest magnitude
3.0Important
Tested on
AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableBadLikely miscall if from Ancestry or Genes for Good; otherwise, possible mutationImportant · 3.0
  2. G;GGoodcommon in clinvarTypical · 0.0

SNPedia records rs121965048 on the minus strand: (A;A), (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Notes

From SNPedia

Notes

T;T

Seen too often in in the data from Ancestry v2 and Genes for Good compared to reported frequency worldwide, so likely to be a miscall in data. If your data is not from Ancestry or Genes for Good, let us know.

Source and license

Adapted from rs121965048 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.