rs3738815
A SNP in the ATP13A2 gene on chromosome 1. Its most notable genotype is C;C: common in clinvar
- Gene
- ATP13A2
- Location
- Chr 116,988,207 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 31%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3738815 on the minus strand: (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.
- AverageC;C 52%
- European ancestry (Utah)C;C 70%
- Han Chinese (Beijing)C;C 18%
- Japanese (Tokyo)C;C 17%
- Yoruba (Nigeria)C;C 83%
- African ancestry (Southwest US)C;C 72%
- Chinese (Denver)C;C 35%
- Gujarati IndianC;C 58%
- Luhya (Kenya)C;C 68%
- Mexican ancestry (Los Angeles)C;C 35%
- Maasai (Kenya)C;C 49%
- TuscanC;C 64%
Related
Other ATP13A2 SNPs
- rs121918227G;GParkinson's mutation, type 9, early-onsetVery important
- rs144701072T;TParkinson's mutation, type 9, early-onsetVery important
- rs199624796A;AParkinson's mutation, type 9, early-onsetVery important
- rs587776890-;-Parkinson's mutation, type 9, early-onsetVery important
- rs587777053G;GParkinson's mutation, type 9, early-onsetVery important
- rs749798211-;-Parkinson's mutation, type 9, early-onsetVery important
- rs762033589TC;TCParkinson's mutation, type 9, early-onsetVery important
- rs786205056T;TParkinson's mutation, type 9, early-onsetVery important
Notes
From SNPedia
Notes
ATP13A2 variability in Parkinson disease.
Source and license
Adapted from rs3738815 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.