{{Rsnum
|rsid=121912566
|Chromosome=4
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NR3C2
|position=148259978
|Gene_s=NR3C2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600983
|rsnum=121912566
|variant=0012
}}{{ClinVar
|rsid=121912566
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=149181130
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NR3C2:4306
|GENE_NAME=NR3C2
|GENE_ID=4306
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.149181130C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600983.0012
|CLNSIG=5
|CLNCUI=C1449842
|CLNDBN=Pseudohypoaldosteronism type 1 autosomal dominant
|Disease=Pseudohypoaldosteronism type 1 autosomal dominant
|CLNACC=RCV000009095.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1449842:177735:171871:756
}}