{{Rsnum
|rsid=4242384
|Chromosome=8
|position=127506309
|Orientation=plus
|GMAF=0.1221
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 86.7 | 12.4 | 0.9
| HCB | 73.7 | 24.1 | 2.2
| JPT | 68.1 | 26.5 | 5.3
| YRI | 65.3 | 32.7 | 2.0
| ASW | 75.4 | 24.6 | 0.0
| CHB | 73.7 | 24.1 | 2.2
| CHD | 78.0 | 17.4 | 4.6
| GIH | 77.2 | 21.8 | 1.0
| LWK | 77.3 | 21.8 | 0.9
| MEX | 89.7 | 10.3 | 0.0
| MKK | 78.2 | 21.2 | 0.6
| TSI | 86.3 | 12.7 | 1.0
| HapMapRevision=28
}}

[http://cancergenetics.wordpress.com/2008/02/15/prostate-cancer-oldnew-snps-and-decodeprca/ cancer-genetics] these snps influence genetic risk for [[prostate cancer]]
*the [[haplotype]] [[rs6983267]] [[rs1016343]] [[rs4242384]] 
*[[rs7501939]] 
*[[rs1859962]]
*[[rs2660753]]
*[[rs9364554]]
*[[rs6465657]]
*[[rs10993994]]
*[[rs7931342]]
*[[rs2735839]]
*[[rs5945619]]
*[[rs10993994]]

{{ neighbor
| rsid = 4242382
| distance = 981
}}

{{PMID Auto GWAS
|PMID=18264097
|Trait=Prostate cancer
|Title=Multiple newly identified loci associated with prostate cancer susceptibility
|RiskAllele=C
|Pval=2.9999999999999999E-16
|OR=1.88
|ORtxt=[NR]
}}
{{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=2E-24
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID Auto GWAS
|PMID=21743057
|Trait=None
|Title=Genome-wide association study identifies new prostate cancer susceptibility loci.
|RiskAllele=C
|Pval=3E-16
|OR=1.5600
|ORtxt=[1.40-1.73]
|OA=1
}}

{{PMID Auto
|PMID=18704501
|Title=Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers.
|OA=1
}}

{{PMID Auto
|PMID=19567509
|Title=Genetic variants and prostate cancer risk: candidate replication and exploration of viral restriction genes.
|OA=1
}}

{{PMID Auto
|PMID=20584312
|Title=8q24 sequence variants in relation to prostate cancer risk among men of African descent: a case-control study.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4242384
|overall_frequency_n=121
|overall_frequency_d=128
|overall_frequency=0.945312
|n_genomes=54
|n_genomes_annotated=0
|n_haplomes=102
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}