rs8177400

A SNP in the TIRAP gene on chromosome 11. Its most notable genotype is A;A.

Gene
TIRAP
Location
Chr 11126,292,695 (GRCh38)
Highest magnitude
3.0Important
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
<1%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableNot ratedNo summary available.Important · 3.00% of people
  2. G;GGoodcommon in complete genomicsTypical · 0.099% of people

On SNPedia: (A;A), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 5 HapMap populations.

  • AverageA;A 0% G;G 99%
  • Han Chinese (Beijing)A;A 0% G;G 98%
  • Japanese (Tokyo)A;A 0% G;G 99%
  • Yoruba (Nigeria)A;A 0% G;G 99%
  • Luhya (Kenya)A;A 0% G;G 98%
  • Mexican ancestry (Los Angeles)A;A 0% G;G 98%

Other TIRAP SNPs

All TIRAP SNPs

Notes

From SNPedia

Notes

A;A

Rare variant

Source and license

Adapted from rs8177400 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.