rs16910526

A SNP in the CLEC7A gene on chromosome 12. Its most notable genotype is C;C.

Gene
CLEC7A
Location
Chr 1210,118,488 (GRCh38)
Highest magnitude
3.0Important
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
3%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableNot ratedNo summary available.Important · 3.00% of people
  2. A;AGoodnormalTypical · 0.092% of people

SNPedia records rs16910526 on the minus strand: (G;G), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 10 HapMap populations.

  • AverageC;C 0% A;A 92%
  • European ancestry (Utah)C;C 0% A;A 84%
  • Han Chinese (Beijing)C;C 0% A;A 99%
  • Japanese (Tokyo)C;C 0% A;A 99%
  • Yoruba (Nigeria)C;C 0% A;A 99%
  • African ancestry (Southwest US)C;C 0% A;A 90%
  • Gujarati IndianC;C 0% A;A 81%
  • Luhya (Kenya)C;C 0% A;A 96%
  • Mexican ancestry (Los Angeles)C;C 0% A;A 88%
  • Maasai (Kenya)C;C 0% A;A 94%
  • TuscanC;C 0% A;A 88%

Notes

From SNPedia

Notes

C;C

omim reports an association with mucocutaneous candidiasis, vulvovaginal candidiasis and onychomycosis

Source and license

Adapted from rs16910526 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.