{{Rsnum
|rsid=137852579
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=AR
|position=67711549
|Gene_s=AR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=313700
|variant=0028
|rsnum=137852579
}}{{ClinVar
|rsid=137852579
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=66931391
|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
|CLNHGVS=NC_000023.10:g.66931391T>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000010506.1
|CLNDBN=Androgen insensitivity, complete
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=313700.0028
|Disease=Androgen insensitivity
}}