rs2280788

A SNP in the CCL5 gene on chromosome 17. Its most notable genotype is G;G.

Gene
CCL5
Location
Chr 1735,880,401 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
4%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodNo summary available.Typical · 0.086% of people
  2. C;CNot ratedNo summary available.Typical · 0.03% of people

SNPedia records rs2280788 on the minus strand: (C;C), (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.

  • AverageG;G 86% C;C 3%
  • European ancestry (Utah)G;G 98% C;C 0%
  • Han Chinese (Beijing)G;G 76% C;C 5%
  • Japanese (Tokyo)G;G 70% C;C 5%
  • Yoruba (Nigeria)G;G 100% C;C 0%

Other CCL5 SNPs

All CCL5 SNPs

Source and license

Adapted from rs2280788 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.