rs11085825

A SNP in the GCDH gene on chromosome 19. Its most notable genotype is C;T: most likely benign polymorphism

Gene
GCDH
Location
Chr 1912,896,644 (GRCh38)
Highest magnitude
1.0Minor
Tested on
23andMe, AncestryDNA, FamilyTreeDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CGoodcommon in clinvarTypical · 0.061% of people
  2. C;TMost notableGoodmost likely benign polymorphismMinor · 1.032% of people
  3. T;TGoodmost likely benign polymorphismMinor · 1.07% of people

On SNPedia: (C;C), (C;T), (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.

  • AverageC;C 61% C;T 32% T;T 7%
  • European ancestry (Utah)C;C 42% C;T 48% T;T 11%
  • Han Chinese (Beijing)C;C 75% C;T 23% T;T 2%
  • Japanese (Tokyo)C;C 71% C;T 27% T;T 2%
  • Yoruba (Nigeria)C;C 76% C;T 24% T;T <1%
  • African ancestry (Southwest US)C;C 70% C;T 23% T;T 7%
  • Chinese (Denver)C;C 74% C;T 23% T;T 3%
  • Gujarati IndianC;C 53% C;T 42% T;T 6%
  • Luhya (Kenya)C;C 69% C;T 29% T;T 2%
  • Mexican ancestry (Los Angeles)C;C 28% C;T 40% T;T 33%
  • Maasai (Kenya)C;C 67% C;T 31% T;T 2%
  • TuscanC;C 49% C;T 38% T;T 13%

Notes

From SNPedia

Notes

aka c.852+223C>T ClinVar indicates "likely pathogenic" (for glutaric aciduria, type 1) according to a single submitter, but with a population frequency as high as 10% for the minor allele homozygote, this seems very unlikely to be correct and instead this variant is most likely not pathogenic.

Source and license

Adapted from rs11085825 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.