rs960089

A SNP on chromosome 8. Its most notable genotype is C;C: common in complete genomics

Gene
None listed
Location
Chr 858,795,750 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
7%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in complete genomicsTypical · 0.085% of people

SNPedia records rs960089 on the minus strand: (G;G). 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 85%
  • European ancestry (Utah)C;C 88%
  • Han Chinese (Beijing)C;C 99%
  • Japanese (Tokyo)C;C 99%
  • Yoruba (Nigeria)C;C 63%
  • African ancestry (Southwest US)C;C 77%
  • Chinese (Denver)C;C 99%
  • Gujarati IndianC;C 90%
  • Luhya (Kenya)C;C 69%
  • Mexican ancestry (Los Angeles)C;C 88%
  • Maasai (Kenya)C;C 76%
  • TuscanC;C 91%

Notes

From SNPedia

Notes

non sig. gwas, hit (p = 6 x 10^-6) for paired associates learning (PAL) total errors at 6 patterns in the CANTAB (Cambridge Neuropsychological Test Automated Battery

Source and license

Adapted from rs960089 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.