{{Rsnum
|rsid=3935740
|Gene=TMC3
|Chromosome=15
|position=81334384
|Orientation=minus
|GMAF=0.2397
|Gene_s=TMC3
|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 | 85.0 | 15.0 | 0.0
| HCB | 55.6 | 41.5 | 3.0
| JPT | 64.3 | 31.2 | 4.5
| YRI | 14.4 | 45.9 | 39.7
| ASW | 17.5 | 63.2 | 19.3
| CHB | 55.6 | 41.5 | 3.0
| CHD | 63.6 | 30.8 | 5.6
| GIH | 69.3 | 30.7 | 0.0
| LWK | 16.5 | 56.9 | 26.6
| MEX | 83.6 | 14.5 | 1.8
| MKK | 21.8 | 51.9 | 26.3
| TSI | 74.5 | 22.5 | 2.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23793441
  |Trait=Parkinson's disease
  |Title=Parkinson disease loci in the mid-western Amish.
  |RiskAllele=T
  |Pval=2E-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}}