{{Rsnum
|rsid=387907168
|Chromosome=1
|position=209707020
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HSD11B1
|Gene_s=HSD11B1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000024294.1
|CLNALLE=1
|CLNDBN=Cortisone reductase deficiency 2
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN125023:614662:ORPHA168588
|CLNHGVS=NC_000001.11:g.209707020C>T
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_181755.2:c.409C>T; 600713.0002
|Disease=Cortisone reductase deficiency 2
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=209707020
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387907168
|GENEINFO=HSD11B1:3290
|GENE_ID=3290
|GENE_NAME=HSD11B1
|CLNORIGIN=1
}}