{{Rsnum
|rsid=80338779
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CACNA1S
|position=201066283
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CACNA1S
}}{{omim
|id=114208
|rsnum=80338779
|variant=0008
}}{{ClinVar
|rsid=80338779
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=201066283
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000a05000002110100
|GENEINFO=CACNA1S:779
|GENE_NAME=CACNA1S
|GENE_ID=779
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.201066283C>A
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000069.2:c.2691G>T; NBK1338; 114208.0008
|CLNSIG=5
|CLNCUI=CN031165; CN031165
|CLNDBN=Hypokalemic periodic paralysis 1
|Disease=Hypokalemic periodic paralysis 1
|CLNACC=RCV000019197.22
|Tags=RV;PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1338:NBK1496:CN031165:170400:ORPHA681
}}{{PMID|18835861}} Early onset of hypokalaemic periodic paralysis caused by a novel mutation of the CACNA1S gene.