{{Rsnum
|rsid=104894147
|Chromosome=10
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CYP17A1
|position=102835350
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP17A1
}}{{omim
|id=609300
|rsnum=104894147
|variant=0019
}}{{ClinVar
|rsid=104894147
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=104595107
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CYP17A1:1586
|GENE_NAME=CYP17A1
|GENE_ID=1586
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.104595107A>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000001865.2
|CLNDBN=Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=609300.0019
|Disease=Complete combined 17-alpha-hydroxylase/17
}}