{{Rsnum
|rsid=7127900
|Chromosome=11
|position=2212344
|Orientation=plus
|GMAF=0.2502
|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 | 6.2 | 34.5 | 59.3
| HCB | 0.7 | 21.2 | 78.1
| JPT | 0.9 | 17.7 | 81.4
| YRI | 16.3 | 46.9 | 36.7
| ASW | 22.8 | 47.4 | 29.8
| CHB | 0.7 | 21.2 | 78.1
| CHD | 1.8 | 13.8 | 84.4
| GIH | 7.9 | 28.7 | 63.4
| LWK | 16.4 | 56.4 | 27.3
| MEX | 15.5 | 44.8 | 39.7
| MKK | 6.4 | 33.3 | 60.3
| TSI | 2.9 | 26.5 | 70.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19767753
|Trait=Prostate cancer
|Title=Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
|RiskAllele=A
|Pval=3E-33
|OR=1.22
|ORtxt=[1.17-1.27]
|OA=1
}}

{{omim
|id=176807
|rsnum=7127900
}}

{{PMID Auto
|PMID=22253814
|Title=A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programme
|OA=1
}}

{{PMID Auto
|PMID=22219177
|Title=A Genome-Wide Search for Loci Interacting with Known Prostate Cancer Risk-Associated Genetic Variants.
|OA=1
}}

{{PMID Auto
|PMID=21390317
|Title=Characterizing associations and SNP-environment interactions for GWAS-identified prostate cancer risk markers--results from BPC3.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7127900
|overall_frequency_n=97
|overall_frequency_d=128
|overall_frequency=0.757812
|n_genomes=51
|n_genomes_annotated=0
|n_haplomes=80
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto
|PMID=24411283
|Title=Prostate Cancer (PCa) Risk Variants and Risk of Fatal PCa in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}