{{Rsnum
|rsid=80338790
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCN4A
|position=63941814
|Gene_s=SCN4A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338790
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=62019174
|CHROM=17
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=SCN4A:6329
|GENE_NAME=SCN4A
|GENE_ID=6329
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.62019174A>G
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK1338; NBK1496
|CLNSIG=5
|CLNCUI=CN031165; CN074266
|CLNDBN=Hypokalemic periodic paralysis 1; Hyperkalemic Periodic Paralysis Type 1
|Disease=Hypokalemic periodic paralysis 1; Hyperkalemic Periodic Paralysis Type 1
|CLNACC=RCV000020274.1; RCV000020275.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1338:NBK1496:CN031165:170400:681; NBK1496:CN074266:170500:682
}}