rs2854386

A SNP in the CXCR1 gene on chromosome 2. Its most notable genotype is C;C: common in complete genomics

Gene
CXCR1
Location
Chr 2218,162,779 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
15%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in complete genomicsTypical · 0.071% of people

SNPedia records rs2854386 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 71%
  • European ancestry (Utah)C;C 89%
  • Han Chinese (Beijing)C;C 80%
  • Japanese (Tokyo)C;C 80%
  • Yoruba (Nigeria)C;C 33%

Other CXCR1 SNPs

All CXCR1 SNPs

Notes

From SNPedia

Notes

Cytokine SNPs: Comparison of allele frequencies by race and implications for future studies.

Source and license

Adapted from rs2854386 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.