rs702966

A SNP in the PHRF1 gene on chromosome 11. Its most notable genotype is C;C: common in complete genomics

Gene
PHRF1
Location
Chr 11611,919 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
28%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in complete genomicsTypical · 0.066% of people

SNPedia records rs702966 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 4 HapMap populations.

  • AverageC;C 66%
  • European ancestry (Utah)C;C 55%
  • Han Chinese (Beijing)C;C 98%
  • Japanese (Tokyo)C;C 96%
  • Yoruba (Nigeria)C;C 16%

Other PHRF1 SNPs

All PHRF1 SNPs

Notes

From SNPedia

Notes

Association of genetic variations in the STAT4 and IRF7/KIAA1542 regions with systemic lupus erythematosus in a Northern Han Chinese population. The role of polymorphisms in Toll-like receptors and their associated intracellular signaling genes in measles vaccine immunity. Novel identification of the IRF7 region as an anticentromere autoantibody propensity locus in systemic sclerosis.

Source and license

Adapted from rs702966 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.