{{Rsnum
|rsid=80338957
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCN4A
|position=63957427
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN4A
}}{{omim
|id=603967
|rsnum=80338957
|variant=0001
}}{{ClinVar
|rsid=80338957
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=62034787
|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.62034787G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1496; 603967.0001
|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=RCV000006254.2; RCV000006255.2; RCV000020267.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C0238357:278513006; NBK1496:CN074266:170500:682
}}