{{Rsnum
|rsid=121912977
|Chromosome=8
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CYP11B2
|position=142914741
|Gene_s=CYP11B2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=124080
|rsnum=121912977
|variant=0006
}}{{ClinVar
|rsid=121912977
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=143996157
|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.143996157C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=124080.0006
|CLNSIG=5
|CLNCUI=CN074214
|CLNDBN=Corticosterone methyloxidase type 1 deficiency
|Disease=Corticosterone methyloxidase type 1 deficiency
|CLNACC=RCV000018376.27
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074214:203400:427
}}