{{Rsnum
|rsid=61757294
|Gene=CYP11B2
|Chromosome=8
|position=142912850
|Orientation=plus
|GMAF=0.04316
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CYP11B2
}}{{omim
|id=124080
|rsnum=61757294
|variant=0001
}}

{{ClinVar
|rsid=61757294
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=143994266
|CHROM=8
|GMAF=0.043
|dbSNPBuildID=129
|SSR=1
|SAO=0
|VP=0x050360000000150116110100
|GENEINFO=CYP11B2:1585
|GENE_NAME=CYP11B2
|GENE_ID=1585
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.143994266A>G
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=124080.0001; 124080.0002
|CLNSIG=5
|CLNCUI=CN074247
|CLNDBN=Corticosterone methyloxidase type 2 deficiency; Corticosterone methyloxidase type 1 deficiency
|Disease=Corticosterone methyloxidase type 2 deficiency; Corticosterone methyloxidase type 1 deficiency
|CLNACC=RCV000018372.26; RCV000018373.26
|Tags=PM;S3D;SLO;VLD;G5;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9568; 0.04316
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074247:610600:427; CN074214:203400:427
|COMMON=1
}}

{{GET Evidence
|gene=CYP11B2
|aa_change=Val386Ala
|aa_change_short=V386A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs61757294
|overall_frequency_n=682
|overall_frequency_d=10756
|overall_frequency=0.0634065
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=2
|autoscore=2
|n_web_uneval=10
}}

{{on chip | 23andMe v3}}