{{Rsnum
|rsid=17497526
|Gene=COL13A1
|Chromosome=10
|position=71580120
|Orientation=plus
|GMAF=0.06933
|Gene_s=COL13A1
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 18.6 | 80.5
| HCB | 0.0 | 17.5 | 82.5
| JPT | 0.0 | 19.5 | 80.5
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.0 | 17.5 | 82.5
| CHD | 0.0 | 16.5 | 83.5
| GIH | 0.0 | 5.0 | 95.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 12.1 | 87.9
| MKK | 0.0 | 0.6 | 99.4
| TSI | 0.0 | 19.6 | 80.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23793441
  |Trait=Parkinson's disease
  |Title=Parkinson disease loci in the mid-western Amish.
  |RiskAllele=G
  |Pval=6E-7
  |OR=NR
  |ORtxt=NR
  }}

{{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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}