{{Rsnum
|rsid=121908560
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=SCN4A
|position=63944694
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN4A
}}{{omim
|id=603967
|rsnum=121908560
|variant=0027
}}{{ClinVar
|rsid=121908560
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=62022054
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SCN4A:6329
|GENE_NAME=SCN4A
|GENE_ID=6329
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.62022054G>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000006285.2
|CLNDBN=Paramyotonia congenita/hyperkalemic periodic paralysis
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603967.0027
|Disease=Paramyotonia congenita/hyperkalemic periodic paralysis
}}