rs137853051
A SNP in the PARK7 gene on chromosome 1. Its most notable genotype is T;T: Parkinson's disease, type 7, early-onset
- Gene
- PARK7
- Location
- Chr 17,965,348 (GRCh38)
- Highest magnitude
- 8.7Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- G;TBadCarrier of an early-onset Parkinson's mutation
- T;TMost notableBadParkinson's disease, type 7, early-onset
On SNPedia: (G;G), (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other PARK7 SNPs
- rs28938172C;CParkinson's disease, type 7, early-onsetVery important
- rs74315351A;AParkinson's disease, type 7, early-onsetVery important
- rs74315352C;CParkinson's disease, type 7, early-onsetVery important
- rs74315353C;CParkinson's disease, type 7, early-onsetVery important
- rs74315354A;AParkinson's disease, type 7, early-onset (likely)Very important
Notes
From SNPedia
Notes
c.115G>T (p.Ala39Ser) 23andMe names this i5047046
G;T
see Parkinson's disease and PARK7
T;T
see Parkinson's disease and PARK7
Source and license
Adapted from rs137853051 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.