rs8003379
A SNP in the MTHFD1 gene on chromosome 14. Its most notable genotype is A;A: normal
- Gene
- MTHFD1
- Location
- Chr 1464,406,881 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 17%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (A;C), (C;C). 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.
- AverageA;A 71% A;C 25% C;C 4%
- European ancestry (Utah)A;A 60% A;C 32% C;C 8%
- Han Chinese (Beijing)A;A 99% A;C 2% C;C 0%
- Japanese (Tokyo)A;A 100% A;C 0% C;C 0%
- Yoruba (Nigeria)A;A 53% A;C 40% C;C 7%
- African ancestry (Southwest US)A;A 65% A;C 30% C;C 5%
- Gujarati IndianA;A 60% A;C 34% C;C 6%
- Luhya (Kenya)A;A 61% A;C 36% C;C 4%
- Mexican ancestry (Los Angeles)A;A 81% A;C 17% C;C 2%
- Maasai (Kenya)A;A 67% A;C 30% C;C 4%
- TuscanA;A 60% A;C 32% C;C 8%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs8003379 is reported to represent a risk factor for abdominal aortic aneurysm (AAA), with odds ratio of 0.41 (CI: 0.26-0.65).
Source and license
Adapted from rs8003379 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.