{{Rsnum
|rsid=9261174
|Gene=NCRNA00171
|Chromosome=6
|position=30029078
|Orientation=plus
|GMAF=0.1846
|Gene_s=ZNRD1-AS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 13.4 | 86.6
| HCB | 2.3 | 35.3 | 62.4
| JPT | 9.0 | 45.0 | 45.9
| YRI | 6.2 | 49.0 | 44.8
| ASW | 3.5 | 52.6 | 43.9
| CHB | 2.3 | 35.3 | 62.4
| CHD | 4.6 | 18.3 | 77.1
| GIH | 1.0 | 20.2 | 78.8
| LWK | 6.5 | 41.7 | 51.9
| MEX | 8.6 | 39.7 | 51.7
| MKK | 5.8 | 44.2 | 50.0
| TSI | 1.0 | 35.3 | 63.7
| HapMapRevision=28
}}

{{omim
|desc=HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
|id=609423
|rsnum=9261174
}}

{{PharmGKB
|RSID=rs9261174
|Name_s=
|Gene_s=ETF1P1
|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=PA162316694
}}

{{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=18982067
|Title=HIV-1 disease-influencing effects associated with ZNRD1, HCP5 and HLA-C alleles are attributable mainly to either HLA-A10 or HLA-B*57 alleles.
|OA=1
}}

{{PMID Auto
|PMID=19107206
|Title=Distinct genetic loci control plasma HIV-RNA and cellular HIV-DNA levels in HIV-1 infection: the ANRS Genome Wide Association 01 study.
|OA=1
}}

{{PMID Auto
|PMID=19679225
|Title=X chromosomal variation is associated with slow progression to AIDS in HIV-1-infected women.
|OA=1
}}

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

{{PMID Auto
|PMID=20552027
|Title=Host and viral genetic correlates of clinical definitions of HIV-1 disease progression.
|OA=1
}}

{{PMID Auto
|PMID=22474614
|Title=Host Genes Important to HIV Replication and Evolution.
|OA=1
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9261174
|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}}