rs9384
A SNP in the GCDH gene on chromosome 19. Its most notable genotype is G;G: common in clinvar
- Gene
- GCDH
- Location
- Chr 1912,899,829 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). 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 55%
- European ancestry (Utah)G;G 42%
- Han Chinese (Beijing)G;G 75%
- Japanese (Tokyo)G;G 70%
- Yoruba (Nigeria)G;G 65%
- African ancestry (Southwest US)G;G 47%
- Chinese (Denver)G;G 71%
- Gujarati IndianG;G 53%
- Luhya (Kenya)G;G 53%
- Mexican ancestry (Los Angeles)G;G 28%
- Maasai (Kenya)G;G 55%
- TuscanG;G 49%
Related
Other GCDH SNPs
- rs121434367T;Tglutaric acidemia type IVery important
- rs121434366C;TCarrier of a Glutaric aciduria type I mutationImportant
- rs121434368C;TCarrier of a Glutaric aciduria type I mutationImportant
- rs142967670A;CCarrier of a Glutaric aciduria type I mutationImportant
- rs199999619A;CCarrier of a Glutaric aciduria type I mutationImportant
- rs566417795A;GCarrier of a Glutaric aciduria type I mutationImportant
- rs752334462C;TCarrier of a Glutaric aciduria type I mutationImportant
- rs777201305A;GCarrier of a Glutaric aciduria type I mutationImportant
Source and license
Adapted from rs9384 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.