rs891835

A SNP in the CCDC26 gene on chromosome 8. Its most notable genotype is G;G.

Gene
CCDC26
Location
Chr 8129,479,506 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
16%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableBadNo summary available.Typical · 0.02% of people
  2. T;TNot ratedNo summary available.Typical · 0.080% of people

On SNPedia: (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 11 HapMap populations.

  • AverageG;G 2% T;T 80%
  • European ancestry (Utah)G;G 4% T;T 66%
  • Han Chinese (Beijing)G;G 3% T;T 76%
  • Japanese (Tokyo)G;G <1% T;T 69%
  • Yoruba (Nigeria)G;G 0% T;T 98%
  • African ancestry (Southwest US)G;G 0% T;T 93%
  • Chinese (Denver)G;G 2% T;T 73%
  • Gujarati IndianG;G 1% T;T 85%
  • Luhya (Kenya)G;G 0% T;T 99%
  • Mexican ancestry (Los Angeles)G;G 3% T;T 64%
  • Maasai (Kenya)G;G 0% T;T 87%
  • TuscanG;G 5% T;T 65%

Other CCDC26 SNPs

All CCDC26 SNPs

Notes

From SNPedia

Notes

G;G

Risk Allele: G

Source and license

Adapted from rs891835 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.