{{Rsnum
|rsid=104894152
|Chromosome=10
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CYP17A1
|position=102837281
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP17A1
}}{{omim
|id=609300
|rsnum=104894152
|variant=0028
}}{{ClinVar
|rsid=104894152
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=104597038
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CYP17A1:1586
|GENE_NAME=CYP17A1
|GENE_ID=1586
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.104597038G>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000001874.1
|CLNDBN=Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=609300.0028
|Disease=Complete combined 17-alpha-hydroxylase/17
}}