{{Rsnum
|rsid=137852708
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCNN1B
|position=23380727
|Gene_s=SCNN1B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600760
|variant=0007
|rsnum=137852708
}}{{ClinVar
|rsid=137852708
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=23392048
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SCNN1B:6338
|GENE_NAME=SCNN1B
|GENE_ID=6338
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.23392048C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600760.0007
|CLNSIG=5
|CLNCUI=C0221043
|CLNDBN=Pseudoprimary hyperaldosteronism
|Disease=Pseudoprimary hyperaldosteronism
|CLNACC=RCV000009384.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0221043:177200:526:71275003
}}