{{Rsnum
|rsid=137852706
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCNN1B
|position=23348708
|Gene_s=SCNN1B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600760
|variant=0003
|rsnum=137852706
}}{{ClinVar
|rsid=137852706
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=23360029
|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.23360029G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600760.0003
|CLNSIG=5
|CLNCUI=C1449843
|CLNDBN=Pseudohypoaldosteronism type 1 autosomal recessive
|Disease=Pseudohypoaldosteronism type 1 autosomal recessive
|CLNACC=RCV000009380.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1449843:264350:171876:756
}}