{{Rsnum
|rsid=121918631
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCN1A
|position=166056450
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN1A
}}{{omim
|id=182389
|rsnum=121918631
|variant=0015
}}
{{omim
|id=604403
|rsnum=121918631
}}{{ClinVar
|rsid=121918631
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=166912960
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=SCN1A:6323
|GENE_NAME=SCN1A
|GENE_ID=6323
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.166912960A>G
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=182389.0015; VAR_025366
|CLNSIG=5
|CLNCUI=C1858673
|CLNDBN=Generalized epilepsy with febrile seizures plus, type 2
|Disease=Generalized epilepsy with febrile seizures plus
|CLNACC=RCV000013758.22
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1318:C1858673:604403:36387
}}{{PMID Auto
|PMID=16326807
|Title=Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures.
|OA=1
}}