{{Rsnum
|rsid=80338958
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN4A
|position=63945614
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN4A
}}{{omim
|id=603967
|rsnum=80338958
|variant=0005
}}{{ClinVar
|rsid=80338958
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=62022974
|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.62022974C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1496; 603967.0005
|CLNSIG=5
|CLNCUI=CN074266
|CLNDBN=Paramyotonia congenita/hyperkalemic periodic paralysis; Hyperkalemic Periodic Paralysis Type 1
|Disease=Paramyotonia congenita/hyperkalemic periodic paralysis; Hyperkalemic Periodic Paralysis Type 1
|CLNACC=RCV000006260.2; RCV000020271.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1496:CN074266:170500:682
}}