{{Rsnum
|rsid=130067
|Gene=CCHCR1
|Chromosome=6
|position=31150734
|Orientation=minus
|GMAF=0.2447
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CCHCR1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 65.5 | 23.9 | 10.6
| HCB | 50.0 | 41.9 | 8.1
| JPT | 48.7 | 40.7 | 10.6
| YRI | 63.3 | 32.7 | 4.1
| ASW | 64.9 | 33.3 | 1.8
| CHB | 50.0 | 41.9 | 8.1
| CHD | 51.4 | 36.7 | 11.9
| GIH | 68.3 | 30.7 | 1.0
| LWK | 66.4 | 30.0 | 3.6
| MEX | 60.3 | 29.3 | 10.3
| MKK | 66.0 | 29.5 | 4.5
| TSI | 70.6 | 28.4 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21743467
|Trait=None
|Title=Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.
|RiskAllele=G
|Pval=3E-8
|OR=1.0500
|ORtxt=[1.02-1.09]
|OA=1
}}

{{GET Evidence
|gene=CCHCR1
|aa_change=Glu364Asp
|aa_change_short=E364D
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs130067
|overall_frequency_n=1469
|overall_frequency_d=7524
|overall_frequency=0.195242
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=19
|n_articles=0
|n_articles_annotated=0
|nblosum100=-2
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=22985493
|Title=Common genetic variants associated with disease from genome-wide association studies are mutually exclusive in prostate cancer and rheumatoid arthritis.
}}

{{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}}