{{Rsnum
|rsid=5736
|Gene=SCNN1G
|Chromosome=16
|position=23189600
|Orientation=plus
|GMAF=0.01194
|Gene_s=SCNN1G
|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 | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.0 | 3.4 | 96.6
| ASW | 0.0 | 1.8 | 98.2
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 1.8 | 98.2
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.9 | 15.6 | 83.5
| MEX | 0.0 | 1.8 | 98.2
| MKK | 2.6 | 20.5 | 76.8
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|id=600761
|variant=0005
|rsnum=5736
}}

{{ClinVar
|rsid=5736
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=23200921
|CHROM=16
|GMAF=0.0119
|dbSNPBuildID=52
|SSR=0
|SAO=1
|VP=0x050160000000150517110100
|GENEINFO=SCNN1G:6340
|GENE_NAME=SCNN1G
|GENE_ID=6340
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.23200921G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600761.0005
|CLNSIG=5
|CLNCUI=CN035469
|CLNDBN=Bronchiectasis with or without elevated sweat chloride 3
|Disease=Bronchiectasis with or without elevated sweat chloride 3
|CLNACC=RCV000009376.1
|Tags=PM;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9881; 0.01194
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2751324:613071
|COMMON=1
}}

{{GET Evidence
|gene=SCNN1G
|aa_change=Gly183Ser
|aa_change_short=G183S
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=other
|quality_scores=Array
|dbsnp_id=rs5736
|overall_frequency_n=132
|overall_frequency_d=10758
|overall_frequency=0.0122699
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=2
|n_articles_annotated=2
|qualityscore_case_control=0
|qualitycomment_case_control=Y
|qualityscore_severity=1
|qualitycomment_severity=Y
|gene_in_genetests=Y
|in_omim=Y
|genetests_testable=Y
|nblosum100=2
|autoscore=4
|webscore=N
|n_web_uneval=1
|summary_short=This variant is associated with weak gain-of-function effect leading to bronchiectasis in one female of African origin.
}}

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