{{Rsnum
|rsid=137853342
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCNN1G
|position=23215237
|Gene_s=SCNN1G
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600761
|variant=0001
|rsnum=137853342
}}{{ClinVar
|rsid=137853342
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=23226558
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SCNN1G:6340
|GENE_NAME=SCNN1G
|GENE_ID=6340
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.23226558G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600761.0001
|CLNSIG=5
|CLNCUI=C0221043
|CLNDBN=Pseudoprimary hyperaldosteronism
|Disease=Pseudoprimary hyperaldosteronism
|CLNACC=RCV000009372.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0221043:177200:526:71275003
}}