rs13182402
A SNP in the ALDH7A1 gene on chromosome 5. Its most notable genotype is A;A: common in complete genomics
- Gene
- ALDH7A1
- Location
- Chr 5126,582,456 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 11%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). 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.
- AverageA;A 76%
- European ancestry (Utah)A;A 81%
- Han Chinese (Beijing)A;A 92%
- Japanese (Tokyo)A;A 97%
- Yoruba (Nigeria)A;A 57%
- African ancestry (Southwest US)A;A 68%
- Chinese (Denver)A;A 89%
- Gujarati IndianA;A 76%
- Luhya (Kenya)A;A 56%
- Mexican ancestry (Los Angeles)A;A 81%
- Maasai (Kenya)A;A 61%
- TuscanA;A 75%
Related
Other ALDH7A1 SNPs
- rs121912707C;GCarrier of a pyridoxine-dependent epilepsy mutationImportant
- rs121912708A;GCarrier of a pyridoxine-dependent epilepsy mutationImportant
- rs121912709A;GCarrier of a pyridoxine-dependent epilepsy mutationImportant
- rs121912710A;CCarrier of a pyridoxine-dependent epilepsy mutationImportant
- rs121912711A;TCarrier of a pyridoxine-dependent epilepsy mutationImportant
- rs140102105C;GCarrier of a pyridoxine-dependent epilepsy mutationImportant
- rs140845195A;CCarrier of a pyridoxine-dependent epilepsy mutationImportant
- rs144701796A;TCarrier of a pyridoxine-dependent epilepsy mutationImportant
Source and license
Adapted from rs13182402 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.