rs1043424
A SNP in the PINK1 gene on chromosome 1. Its most notable genotype is A;A: common in clinvar
- Gene
- PINK1
- Location
- Chr 120,650,507 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 28%
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 51%
- European ancestry (Utah)A;A 51%
- Han Chinese (Beijing)A;A 39%
- Japanese (Tokyo)A;A 52%
- Yoruba (Nigeria)A;A 64%
- African ancestry (Southwest US)A;A 53%
- Chinese (Denver)A;A 37%
- Gujarati IndianA;A 37%
- Luhya (Kenya)A;A 59%
- Mexican ancestry (Los Angeles)A;A 59%
- Maasai (Kenya)A;A 59%
- TuscanA;A 57%
Related
Other PINK1 SNPs
- rs28940284A;AParkinson's disease, type 6, early-onsetVery important
- rs28940285C;CParkinson's disease, type 6, early-onsetVery important
- rs45539432T;TParkinson's disease, type 6, early-onset; likelyVery important
- rs74315355A;AParkinson's disease, type 6, early-onsetVery important
- rs74315356A;AParkinson's disease, type 6, early-onsetVery important
- rs74315357T;TParkinson's disease, type 6, early-onsetVery important
- rs74315358A;AParkinson's disease, type 6, early-onsetVery important
- rs74315359T;TParkinson's disease, type 6, early-onsetVery important
Source and license
Adapted from rs1043424 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.