{{Rsnum
|rsid=7617877
|Gene=CCDC61
|Chromosome=3
|position=28664273
|Orientation=plus
|GMAF=0.3365
|Gene_s=CCDC61
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 14.3 | 42.0 | 43.8
| HCB | 0.7 | 35.8 | 63.5
| JPT | 5.3 | 48.7 | 46.0
| YRI | 23.1 | 52.4 | 24.5
| ASW | 19.3 | 49.1 | 31.6
| CHB | 0.7 | 35.8 | 63.5
| CHD | 9.3 | 26.2 | 64.5
| GIH | 25.7 | 50.5 | 23.8
| LWK | 31.2 | 46.8 | 22.0
| MEX | 8.9 | 26.8 | 64.3
| MKK | 17.9 | 47.4 | 34.6
| TSI | 14.1 | 49.5 | 36.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21044948
|Trait=None
|Title=Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
|RiskAllele=A
|Pval=0.000003
|OR=1.2300
|ORtxt=[1.13-1.33]
|OA=1
}}

{{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 | Illumina Human 1M}}