rs6136

A SNP in the SELP gene on chromosome 1. Its most notable genotype is T;T: common

Gene
SELP
Location
Chr 1169,594,713 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
4%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommonTypical · 0.095% of people
  2. G;TNot ratedNo summary available.Typical · 0.04% of people
  3. G;GNot ratedNo summary available.Typical · 0.01% of people
  4. A;ANot ratedNo summary available.Typical · 0.00% of people

SNPedia records rs6136 on the minus strand: (A;A), (A;C), (C;C), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 6 HapMap populations.

  • AverageT;T 95% G;T 4% G;G 1% A;A 0%
  • European ancestry (Utah)T;T 80% G;T 20% G;G 0% A;A 0%
  • Han Chinese (Beijing)T;T 98% G;T 2% G;G 0% A;A 0%
  • Japanese (Tokyo)T;T 100% G;T 0% G;G 0% A;A 0%
  • Yoruba (Nigeria)T;T 100% G;T 0% G;G 0% A;A 0%
  • African ancestry (Southwest US)T;T 95% G;T 2% G;G 4% A;A 0%
  • Gujarati IndianT;T 95% G;T 2% G;G 3% A;A 0%

Other SELP SNPs

All SELP SNPs

Notes

From SNPedia

Notes

cardiovascular risk

Source and license

Adapted from rs6136 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.