{{Rsnum
|rsid=121908546
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCN4A
|position=63951866
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN4A
}}{{omim
|id=603967
|rsnum=121908546
|variant=0006
}}{{ClinVar
|rsid=121908546
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=62029226
|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.62029226G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603967.0006
|CLNSIG=5
|CLNCUI=C0752355
|CLNDBN=Paramyotonia congenita/myotonia congenita; Potassium aggravated myotonia
|Disease=Paramyotonia congenita/myotonia congenita; Potassium aggravated myotonia
|CLNACC=RCV000006261.2; RCV000006262.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet:Orphanet
|CLNDSDBID=NBK1338:C0752355:608390:612:99734:99735:99736
}}