{{Rsnum
|rsid=2074479
|Gene=RNF39
|Chromosome=6
|position=30073232
|Orientation=minus
|GMAF=0.1846
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=RNF39
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 13.3 | 85.8
| HCB | 2.2 | 35.0 | 62.8
| JPT | 8.8 | 45.1 | 46.0
| YRI | 6.8 | 49.0 | 44.2
| ASW | 3.5 | 52.6 | 43.9
| CHB | 2.2 | 35.0 | 62.8
| CHD | 4.6 | 18.3 | 77.1
| GIH | 2.0 | 19.8 | 78.2
| LWK | 6.4 | 42.7 | 50.9
| MEX | 8.6 | 39.7 | 51.7
| MKK | 6.4 | 43.6 | 50.0
| TSI | 1.0 | 35.3 | 63.7
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs2074479
|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=PA162316697
}}

{{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
|gene=RNF39
|aa_change=Ser203Pro
|aa_change_short=S203P
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2074479
|overall_frequency_n=1327
|overall_frequency_d=7524
|overall_frequency=0.176369
|n_genomes=25
|n_genomes_annotated=0
|n_haplomes=30
|n_articles=1
|n_articles_annotated=1
|in_pharmgkb=Y
|nblosum100=3
|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}}