{{Rsnum
|rsid=121908548
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN4A
|position=63941517
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN4A
}}{{omim
|id=603967
|rsnum=121908548
|variant=0009
}}{{ClinVar
|rsid=121908548
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=62018877
|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.62018877C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603967.0009
|CLNSIG=5
|CLNCUI=C0752355
|CLNDBN=Potassium aggravated myotonia; Paramyotonia congenita
|Disease=Potassium aggravated myotonia; Paramyotonia congenita
|CLNACC=RCV000006267.2; RCV000006268.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet:Orphanet
|CLNDSDBID=NBK1338:C0752355:608390:612:99734:99735:99736
}}