{{Rsnum
|rsid=9332971
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=AR
|position=67722944
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AR
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|id=313700
|rsnum=9332971
|variant=0019
}}

{{ClinVar
|rsid=9332971
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=66942786
|CHROM=X
|dbSNPBuildID=119
|SSR=0
|SAO=1
|VP=0x050260000000040503110101
|GENEINFO=AR:367
|GENE_NAME=AR
|GENE_ID=367
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.66942786G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=313700.0019
|CLNSIG=5
|CLNCUI=C0268301
|CLNDBN=Reifenstein syndrome
|Disease=Reifenstein syndrome
|CLNACC=RCV000010497.1
|Tags=PM;S3D;VLD;HD;GNO;OTHERKG;PH3;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268301:312300:90797:58672003
}}

{{on chip | Illumina Human 1M}}