rs609320

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

Gene
RHCE
Location
Chr 125,390,874 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
16%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.073% 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 73%
  • European ancestry (Utah)C;C 75%
  • Han Chinese (Beijing)C;C 57%
  • Japanese (Tokyo)C;C 53%
  • Yoruba (Nigeria)C;C 85%
  • African ancestry (Southwest US)C;C 75%
  • Chinese (Denver)C;C 56%
  • Gujarati IndianC;C 90%
  • Luhya (Kenya)C;C 90%
  • Mexican ancestry (Los Angeles)C;C 60%
  • Maasai (Kenya)C;C 93%
  • TuscanC;C 71%

Notes

From SNPedia

Notes

DNA-based methods in the immunohematology reference laboratory. Rh E/e blood group

Source and license

Adapted from rs609320 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.