rs868014

A SNP in the C1orf167 gene on chromosome 1. Its most notable genotype is A;A: common in clinvar

Gene
C1orf167
Location
Chr 111,789,390 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in clinvarTypical · 0.02% of people

SNPedia records rs868014 on the minus strand: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 4 HapMap populations.

  • AverageA;A 2%
  • European ancestry (Utah)A;A 0%
  • Han Chinese (Beijing)A;A 0%
  • Japanese (Tokyo)A;A 0%
  • Yoruba (Nigeria)A;A 7%

Other C1orf167 SNPs

All C1orf167 SNPs

Source and license

Adapted from rs868014 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.