{{Rsnum
|rsid=121912979
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CYP11B2
|position=142914404
|Gene_s=CYP11B2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=124080
|rsnum=121912979
|variant=0013
}}{{ClinVar
|rsid=121912979
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=143995820
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CYP11B2:1585
|GENE_NAME=CYP11B2
|GENE_ID=1585
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.143995820G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=124080.0013
|CLNSIG=5
|CLNCUI=CN074247
|CLNDBN=Corticosterone methyloxidase type 2 deficiency
|Disease=Corticosterone methyloxidase type 2 deficiency
|CLNACC=RCV000018382.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074247:610600:427
}}