{{Rsnum
|rsid=10761581
|Gene=NCOA4
|Chromosome=10
|position=51568378
|Orientation=plus
|GMAF=0.41
|Gene_s=NCOA4,TIMM23B
|Assembly=GRCh37.p2
|GenomeBuild=37.2
|dbSNPBuild=134
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 23.9 | 46.0 | 30.1
| HCB | 30.7 | 43.8 | 25.5
| JPT | 23.9 | 58.4 | 17.7
| YRI | 7.5 | 43.2 | 49.3
| ASW | 17.5 | 35.1 | 47.4
| CHB | 30.7 | 43.8 | 25.5
| CHD | 26.6 | 52.3 | 21.1
| GIH | 50.5 | 40.6 | 8.9
| LWK | 6.4 | 40.0 | 53.6
| MEX | 8.6 | 46.6 | 44.8
| MKK | 8.3 | 44.2 | 47.4
| TSI | 21.6 | 49.0 | 29.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=20717903
|Title=Evidence for an association between prostate cancer and chromosome 8q24 and 10q11 genetic variants in African American men: The flint men's health study
}}

{{PMID Auto
|PMID=19153072
|Title=Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk.
|OA=1
}}

{{PMID Auto
|PMID=19644707
|Title=Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer.
|OA=1
}}

{{GET Evidence
|gene=NCOA4
|aa_change=Phe8Val
|aa_change_short=F8V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10761581
|overall_frequency_n=1366
|overall_frequency_d=3234
|overall_frequency=0.422387
|n_genomes=3
|n_genomes_annotated=0
|n_haplomes=3
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}