{{Rsnum
|rsid=80338962
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN4A
|position=63941508
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN4A
}}{{omim
|id=603967
|rsnum=80338962
|variant=0002
}}{{ClinVar
|rsid=80338962
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=62018868
|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.62018868T>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1496; 603967.0002
|CLNSIG=5
|CLNCUI=CN074266
|CLNDBN=Familial hyperkalemic periodic paralysis; Paramyotonia congenita/hyperkalemic periodic paralysis; Hyperkalemic Periodic Paralysis Type 1
|Disease=Familial hyperkalemic periodic paralysis; Paramyotonia congenita/hyperkalemic periodic paralysis; Hyperkalemic Periodic Paralysis Type 1
|CLNACC=RCV000006256.2; RCV000006257.2; RCV000020279.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C0238357:278513006; NBK1496:CN074266:170500:682
}}