{{Rsnum
|rsid=137852634
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCNN1A
|position=6348981
|Gene_s=SCNN1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600228
|variant=0002
|rsnum=137852634
}}{{ClinVar
|rsid=137852634
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=6458147
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SCNN1A:6337
|GENE_NAME=SCNN1A
|GENE_ID=6337
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.6458147G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600228.0002
|CLNSIG=5
|CLNCUI=C1449843
|CLNDBN=Pseudohypoaldosteronism type 1 autosomal recessive
|Disease=Pseudohypoaldosteronism type 1 autosomal recessive
|CLNACC=RCV000009846.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1449843:264350:171876:756
}}