rs3765129

A SNP in the ABCC1 gene on chromosome 16. Its most notable genotype is C;C.

Gene
ABCC1
Location
Chr 1616,056,044 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
11%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableNot ratedNo summary available.Typical · 0.084% 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 84%
  • European ancestry (Utah)C;C 69%
  • Han Chinese (Beijing)C;C 77%
  • Japanese (Tokyo)C;C 83%
  • Yoruba (Nigeria)C;C 97%
  • African ancestry (Southwest US)C;C 93%
  • Chinese (Denver)C;C 83%
  • Gujarati IndianC;C 88%
  • Luhya (Kenya)C;C 96%
  • Mexican ancestry (Los Angeles)C;C 67%
  • Maasai (Kenya)C;C 97%
  • TuscanC;C 78%

Other ABCC1 SNPs

All ABCC1 SNPs

Notes

From SNPedia

Notes

Nucleotide sequence analyses of the MRP1 gene in four populations suggest negative selection on its coding region.

Source and license

Adapted from rs3765129 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.