{{Rsnum
|rsid=121434319
|Chromosome=10
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TTC)
|geno3=(TTC;TTC)
|Gene=CYP17A1
|position=102837203
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP17A1
}}{{omim
|id=609300
|rsnum=121434319
|variant=0002
}}{{ClinVar
|rsid=121434319
|Reversed=1
|FwdREF=TTC
|FwdALT=
|REF=TGAA
|ALT=T
|RSPOS=104596956
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110200
|GENEINFO=CYP17A1:1586
|GENE_NAME=CYP17A1
|GENE_ID=1586
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.104596960_104596962delGAA
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000001850.1
|CLNDBN=Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=609300.0002
|Disease=Combined partial 17-alpha-hydroxylase/17
}}