{{Rsnum
|rsid=193922393
|Chromosome=8
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=STAR
|position=38148684
|Gene_s=STAR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922393
|Reversed=1
|FwdREF=T
|FwdALT=
|REF=TA
|ALT=T
|RSPOS=38006201
|CHROM=8
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.38006202delA
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Cholesterol monooxygenase (side-chain cleaving) deficiency
|Disease=Cholesterol monooxygenase (side-chain cleaving) deficiency
|Tags=RV;PM;PMC;OTHERKG;LSD
|CLNACC=RCV000030462.1
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0342474:201710:418:44231009
|GENEINFO=STAR:6770
|GENE_ID=6770
|GENE_NAME=STAR
}}{{PMID|9141542}} Spontaneous feminization in a 46,XX female patient with congenital lipoid adrenal hyperplasia due to a homozygous frameshift mutation in the steroidogenic acute regulatory protein.

{{PMID|10486704}} Congenital adrenal hyperplasia: molecular genetics and alternative approaches to treatment.