rs602633

A SNP on chromosome 1. Its most notable genotype is T;T.

Gene
None listed
Location
Chr 1109,278,889 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableNot ratedNo summary available.Typical · 0.023% of people
  2. G;TNot ratedNo summary available.Typical · 0.028% of people
  3. G;GNot ratedNo summary available.Typical · 0.048% of people

SNPedia records rs602633 on the minus strand: (A;A), (A;C), (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageT;T 23% G;T 28% G;G 48%
  • European ancestry (Utah)T;T 11% G;T 38% G;G 52%
  • Han Chinese (Beijing)T;T 0% G;T 11% G;G 89%
  • Japanese (Tokyo)T;T 2% G;T 12% G;G 86%
  • Yoruba (Nigeria)T;T 69% G;T 28% G;G 3%
  • African ancestry (Southwest US)T;T 56% G;T 35% G;G 9%
  • Chinese (Denver)T;T 1% G;T 9% G;G 91%
  • Gujarati IndianT;T 10% G;T 34% G;G 56%
  • Luhya (Kenya)T;T 63% G;T 34% G;G 3%
  • Mexican ancestry (Los Angeles)T;T 4% G;T 32% G;G 64%
  • Maasai (Kenya)T;T 35% G;T 50% G;G 15%
  • TuscanT;T 5% G;T 30% G;G 65%

Source and license

Adapted from rs602633 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.