rs6441961

A SNP in the LOC100131327 gene on chromosome 3. Its most notable genotype is C;C: common/normal

Gene
LOC100131327
Location
Chr 346,310,893 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
27%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon/normalTypical · 0.057% 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 57%
  • European ancestry (Utah)C;C 47%
  • Han Chinese (Beijing)C;C 44%
  • Japanese (Tokyo)C;C 50%
  • Yoruba (Nigeria)C;C 84%
  • African ancestry (Southwest US)C;C 68%
  • Chinese (Denver)C;C 47%
  • Gujarati IndianC;C 42%
  • Luhya (Kenya)C;C 77%
  • Mexican ancestry (Los Angeles)C;C 50%
  • Maasai (Kenya)C;C 69%
  • TuscanC;C 50%

Notes

From SNPedia

Notes

Translational mini-review series on the immunogenetics of gut disease: immunogenetics of coeliac disease. Shared and distinct genetic variants in type 1 diabetes and celiac disease. Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.

Source and license

Adapted from rs6441961 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.