{{Rsnum
|rsid=104894154
|Chromosome=10
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CYP17A1
|position=102835316
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP17A1
}}{{omim
|id=609300
|rsnum=104894154
|variant=0030
}}{{ClinVar
|rsid=104894154
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=104595073
|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.104595073C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000001876.1; RCV000068782.2
|CLNDBN=Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency; Malignant melanoma
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=609300.0030
|Disease=Complete combined 17-alpha-hydroxylase/17; Malignant melanoma
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0025202:2092003
}}