{{Rsnum
|rsid=104894899
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=NR0B1
|position=30308222
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NR0B1
}}{{omim
|id=300473
|rsnum=104894899
|variant=0023
}}{{ClinVar
|rsid=104894899
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=30326339
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NR0B1:190
|GENE_NAME=NR0B1
|GENE_ID=190
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.30326339A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300473.0023
|CLNSIG=5
|CLNCUI=C0342482
|CLNDBN=Congenital adrenal hypoplasia, X-linked
|Disease=Congenital adrenal hypoplasia
|CLNACC=RCV000011718.5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1431:C0342482:300200:237764004
}}