{{Rsnum
|rsid=72554626
|Chromosome=8
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CYP11B2
|position=142912000
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP11B2
}}{{omim
|id=124080
|rsnum=72554626
|variant=0012
}}

{{ClinVar
|rsid=72554626
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=143993416
|CHROM=8
|dbSNPBuildID=130
|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.143993416T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=124080.0012
|CLNSIG=5
|CLNCUI=CN074247
|CLNDBN=Corticosterone methyloxidase type 2 deficiency
|Disease=Corticosterone methyloxidase type 2 deficiency
|CLNACC=RCV000018381.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074247:610600:427
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}