{{Rsnum
|rsid=10799655
|Gene=PINK1
|Chromosome=1
|position=20630938
|Orientation=plus
|GMAF=0.3072
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 60.7 | 35.7 | 3.6
| HCB | 25.4 | 53.0 | 21.6
| JPT | 23.4 | 48.6 | 27.9
| YRI | 37.5 | 47.9 | 14.6
| ASW | 45.5 | 38.2 | 16.4
| CHB | 25.4 | 53.0 | 21.6
| CHD | 18.7 | 55.1 | 26.2
| GIH | 37.4 | 50.5 | 12.1
| LWK | 45.9 | 42.2 | 11.9
| MEX | 52.7 | 41.8 | 5.5
| MKK | 57.4 | 36.8 | 5.8
| TSI | 72.3 | 26.7 | 1.0
| HapMapRevision=28
}}Near the [[PINK1]] gene, this SNP may be related to [[obesity]] and [[diabetes]].

Genomic variants at the [[PINK1]] locus are associated with transcript abundance and plasma nonesterified fatty acid concentrations in European whites. T allele associated with higher [[PINK1]] transcript levels.{{PMID|18495756}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}