rs1801334
A SNP in the PARK2 gene on chromosome 6. Its most notable genotype is C;C: common in clinvar
- Gene
- PARK2
- Location
- Chr 6161,360,193 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 2%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs1801334 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 10 HapMap populations.
- AverageC;C 97%
- European ancestry (Utah)C;C 89%
- Han Chinese (Beijing)C;C 99%
- Japanese (Tokyo)C;C 100%
- Yoruba (Nigeria)C;C 99%
- African ancestry (Southwest US)C;C 93%
- Gujarati IndianC;C 99%
- Luhya (Kenya)C;C 99%
- Mexican ancestry (Los Angeles)C;C 98%
- Maasai (Kenya)C;C 99%
- TuscanC;C 96%
Related
Other PARK2 SNPs
- rs34424986A;AEarly-onset (juvenile) Parkinson's disease likelyVery important
- rs137853054C;CEarly-onset (juvenile) Parkinson's disease likelyVery important
- rs137853055A;AEarly-onset (juvenile) Parkinson's disease likelyVery important
- rs137853056T;TEarly-onset (juvenile) Parkinson's disease likelyVery important
- rs137853057A;AEarly-onset (juvenile) Parkinson's disease likelyVery important
- rs137853058T;TEarly-onset (juvenile) Parkinson's disease likelyVery important
- rs137853059T;TEarly-onset (juvenile) Parkinson's disease likelyVery important
- rs137853060A;AEarly-onset (juvenile) Parkinson's disease likelyVery important
Source and license
Adapted from rs1801334 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.