{{Rsnum
|rsid=121912573
|Chromosome=4
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NR3C2
|position=148152526
|Gene_s=NR3C2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600983
|rsnum=121912573
|variant=0019
}}{{ClinVar
|rsid=121912573
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=149073677
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NR3C2:4306
|GENE_NAME=NR3C2
|GENE_ID=4306
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.149073677G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600983.0019
|CLNSIG=5
|CLNCUI=C1449842
|CLNDBN=Pseudohypoaldosteronism type 1 autosomal dominant
|Disease=Pseudohypoaldosteronism type 1 autosomal dominant
|CLNACC=RCV000009102.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1449842:177735:171871:756
}}