{{Rsnum
|rsid=16851009
|Gene=GALNT3
|Chromosome=2
|position=165774197
|Orientation=plus
|GMAF=0.1814
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=GALNT3,LOC102724230
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 84.5 | 15.5 | 0.0
| HCB | 45.0 | 42.7 | 12.2
| JPT | 55.4 | 32.1 | 12.5
| YRI | 75.9 | 22.8 | 1.4
| ASW | 0.0 | 0.0 | 0.0
| CHB | 45.0 | 42.7 | 12.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 67.0 | 28.9 | 4.1
| LWK | 0.0 | 0.0 | 0.0
| MEX | 49.1 | 41.8 | 9.1
| MKK | 0.0 | 0.0 | 0.0
| TSI | 81.4 | 17.5 | 1.0
| HapMapRevision=28
}}

{{Report GE
|PubMed=16252231
|Source=pubmed
|AffyProbeset=SNP_A-8294813
|AffyOrientation=reverse
|AlleleA=A
|AlleleB=G
|onGW5=
|rsid=16851009
|ancestral=C
|RiskPopulation=
|RiskAllele=T
|CaseFreq=0.13
|ControlFreq=0.08
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.84
|Disease=Parkinson's disease
|DiseaseSymbol=PKD
|OA=1
}}

rs16851009 increases susceptibility to Parkinson's disease 1.84 times for carriers of the T allele {{PMID|16252231|OA=1
}}

{{PMID|16685661|OA=1
}} Genomewide association, Parkinson disease, and PARK10.

{{PMID|16685662|OA=1
}} No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

{{PMID|16685663|OA=1
}} A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}