rs10481151

A SNP on chromosome 8. Its most notable genotype is C;C.

Gene
None listed
Location
Chr 8123,819,594 (GRCh38)
Highest magnitude
1.0Minor
Tested on
23andMe, AncestryDNA
Minor allele frequency
28%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableNot ratedNo summary available.Minor · 1.014% of people

On SNPedia: (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.

  • AverageC;C 14%
  • European ancestry (Utah)C;C 0%
  • Han Chinese (Beijing)C;C 13%
  • Japanese (Tokyo)C;C 7%
  • Yoruba (Nigeria)C;C 39%
  • African ancestry (Southwest US)C;C 19%
  • Chinese (Denver)C;C 12%
  • Gujarati IndianC;C 5%
  • Luhya (Kenya)C;C 27%
  • Mexican ancestry (Los Angeles)C;C 10%
  • Maasai (Kenya)C;C 24%
  • TuscanC;C 1%

Notes

From SNPedia

Notes

non sig. gwas, hit (p = 4 x 10^-7) for pattern recognition memory (PRM) percent correct in the CANTAB (Cambridge Neuropsychological Test Automated Battery)

C;C

supposedly mentioned in one intelligence paper, but no replications in 7 years.

Source and license

Adapted from rs10481151 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.