{{Rsnum
|rsid=3782724
|Gene=SCNN1A
|Chromosome=12
|position=6356915
|Orientation=plus
|GMAF=0.2479
|Gene_s=SCNN1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 90.3 | 9.7 | 0.0
| HCB | 59.1 | 35.0 | 5.8
| JPT | 53.1 | 39.8 | 7.1
| YRI | 15.0 | 45.6 | 39.5
| ASW | 28.1 | 45.6 | 26.3
| CHB | 59.1 | 35.0 | 5.8
| CHD | 65.1 | 29.4 | 5.5
| GIH | 62.4 | 32.7 | 5.0
| LWK | 11.0 | 40.4 | 48.6
| MEX | 89.7 | 8.6 | 1.7
| MKK | 26.3 | 42.9 | 30.8
| TSI | 89.2 | 10.8 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23563609
  |Trait=Obesity (early onset extreme)
  |Title=Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
  |RiskAllele=G
  |Pval=3E-7
  |OR=1.47
  |ORtxt=[1.27-171]
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}