rs9061

A SNP in the SP110 gene on chromosome 2. Its most notable genotype is C;C: common in clinvar

Gene
SP110
Location
Chr 2230,212,395 (GRCh38)
Highest magnitude
0.0Typical
Tested on
Not on consumer chips
Minor allele frequency
12%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.073% of people

SNPedia records rs9061 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 10 HapMap populations.

  • AverageC;C 73%
  • Han Chinese (Beijing)C;C 60%
  • Japanese (Tokyo)C;C 72%
  • Yoruba (Nigeria)C;C 87%
  • African ancestry (Southwest US)C;C 95%
  • Chinese (Denver)C;C 66%
  • Gujarati IndianC;C 51%
  • Luhya (Kenya)C;C 73%
  • Mexican ancestry (Los Angeles)C;C 96%
  • Maasai (Kenya)C;C 58%
  • TuscanC;C 76%

Other SP110 SNPs

All SP110 SNPs

Source and license

Adapted from rs9061 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.