rs669607

A SNP in the LOC107986041 gene on chromosome 3. Its most notable genotype is A;C: common in complete genomics

Gene
LOC107986041
Location
Chr 328,029,953 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
39%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. A;CMost notableGoodcommon in complete genomicsTypical · 0.040% of people

SNPedia records rs669607 on the minus strand: (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.

  • AverageA;C 40%
  • European ancestry (Utah)A;C 37%
  • Han Chinese (Beijing)A;C 54%
  • Japanese (Tokyo)A;C 46%
  • Yoruba (Nigeria)A;C 14%
  • African ancestry (Southwest US)A;C 35%
  • Chinese (Denver)A;C 55%
  • Gujarati IndianA;C 43%
  • Luhya (Kenya)A;C 19%
  • Mexican ancestry (Los Angeles)A;C 51%
  • Maasai (Kenya)A;C 33%
  • TuscanA;C 51%

Conditions, medicines and genes

Notes

From SNPedia

Notes

23andMe blog multiple sclerosis C 1.15x

Source and license

Adapted from rs669607 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.