{{Rsnum
|rsid=137852600
|Chromosome=X
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=AR
|position=67717535
|Gene_s=AR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=313700
|variant=0056
|rsnum=137852600
}}
{{omim
|id=313700
|variant=0057
|rsnum=137852600
}}{{ClinVar
|rsid=137852600
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=66937377
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=AR:367
|GENE_NAME=AR
|GENE_ID=367
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.66937377G>A; NC_000023.10:g.66937377G>T
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000010533.2; RCV000010531.1; RCV000010532.1
|CLNDBN=Androgen insensitivity, complete; Reifenstein syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268301:312300:90797:58672003
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=313700.0057; 313700.0056
|Disease=Androgen insensitivity; Reifenstein syndrome
}}