{{Rsnum
|rsid=2074480
|Gene=RNF39
|Chromosome=6
|position=30073033
|Orientation=minus
|GMAF=0.1846
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=RNF39
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 85.8 | 13.3 | 0.9
| HCB | 63.2 | 34.6 | 2.2
| JPT | 46.0 | 45.1 | 8.8
| YRI | 44.5 | 48.6 | 6.8
| ASW | 43.9 | 52.6 | 3.5
| CHB | 63.2 | 34.6 | 2.2
| CHD | 77.1 | 18.3 | 4.6
| GIH | 78.2 | 19.8 | 2.0
| LWK | 51.4 | 42.2 | 6.4
| MEX | 51.7 | 39.7 | 8.6
| MKK | 50.0 | 43.6 | 6.4
| TSI | 63.7 | 35.3 | 1.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs2074480
|Name_s=
|Gene_s=PPP1R11, RNF39
|Feature=
|Evidence=PubMed ID:17641165
|Annotation=This variant is associated with low HIV viral load and disease progression.
|Drugs=
|Drug Classes=
|Diseases=HIV; HIV Infections
|Curation Level=Curated
|PharmGKB Accession ID=PA162316698
}}

{{PMID Auto
|PMID=18495769
|Title=Transmission of human immunodeficiency virus type 1 from a patient who developed AIDS to an elite suppressor.
|OA=1
}}

{{PMID Auto
|PMID=20041166
|Title=Common genetic variation and the control of HIV-1 in humans.
|OA=1
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2074480
|overall_frequency_n=25
|overall_frequency_d=128
|overall_frequency=0.195312
|n_genomes=24
|n_genomes_annotated=0
|n_haplomes=29
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}