rs1065341

A SNP in the CCL5 gene on chromosome 17. Its most notable genotype is T;T: common in complete genomics

Gene
CCL5
Location
Chr 1735,871,589 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
8%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in complete genomicsTypical · 0.078% of people

SNPedia records rs1065341 on the minus strand: (A;A). 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.

  • AverageT;T 78%
  • European ancestry (Utah)T;T 90%
  • Han Chinese (Beijing)T;T 96%
  • Japanese (Tokyo)T;T 100%
  • Yoruba (Nigeria)T;T 49%
  • African ancestry (Southwest US)T;T 71%
  • Chinese (Denver)T;T 99%
  • Gujarati IndianT;T 68%
  • Luhya (Kenya)T;T 49%
  • Mexican ancestry (Los Angeles)T;T 93%
  • Maasai (Kenya)T;T 45%
  • TuscanT;T 92%

Other CCL5 SNPs

All CCL5 SNPs

Source and license

Adapted from rs1065341 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.