rs508001

A SNP in the CRTAC1 gene on chromosome 10. Its most notable genotype is A;A: common in complete genomics

Gene
CRTAC1
Location
Chr 1097,995,216 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
16%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in complete genomicsTypical · 0.064% of people

On SNPedia: (A;A). 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.

  • AverageA;A 64%
  • European ancestry (Utah)A;A 74%
  • Han Chinese (Beijing)A;A 76%
  • Japanese (Tokyo)A;A 81%
  • Yoruba (Nigeria)A;A 44%
  • African ancestry (Southwest US)A;A 58%
  • Chinese (Denver)A;A 84%
  • Gujarati IndianA;A 63%
  • Luhya (Kenya)A;A 36%
  • Mexican ancestry (Los Angeles)A;A 85%
  • Maasai (Kenya)A;A 31%
  • TuscanA;A 73%

Notes

From SNPedia

Notes

Mentioned in retracted

A;A

http://www.diygenomics.org/webapp/gen_data.php

Source and license

Adapted from rs508001 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.