rs1129187

A SNP in the PEX6 gene on chromosome 6. Its most notable genotype is G;G: common in clinvar

Gene
PEX6
Location
Chr 642,964,462 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
33%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in clinvarTypical · 0.049% of people
  2. A;CNot ratedNo summary available.Typical · 0.00% of people

SNPedia records rs1129187 on the minus strand: (C;C), (G;T). 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.

  • AverageG;G 49% A;C 0%
  • European ancestry (Utah)G;G 32% A;C 0%
  • Han Chinese (Beijing)G;G 82% A;C 0%
  • Japanese (Tokyo)G;G 73% A;C 0%
  • Yoruba (Nigeria)G;G 44% A;C 0%
  • African ancestry (Southwest US)G;G 49% A;C 0%
  • Chinese (Denver)G;G 75% A;C 0%
  • Gujarati IndianG;G 42% A;C 0%
  • Luhya (Kenya)G;G 41% A;C 0%
  • Mexican ancestry (Los Angeles)G;G 50% A;C 0%
  • Maasai (Kenya)G;G 28% A;C 0%
  • TuscanG;G 27% A;C 0%

Source and license

Adapted from rs1129187 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.