{{Rsnum
|rsid=121917955
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SCN1A
|position=165992307
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC102724058,LOC102724067,SCN1A
}}{{omim
|id=182389
|rsnum=121917955
|variant=0005
}}
{{omim
|id=604233
|rsnum=121917955
}}{{ClinVar
|rsid=121917955
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=166848817
|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.166848817G>C
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=0
|CLNSRCID=182389.0005; VAR_014273
|CLNSIG=5
|CLNCUI=C1858673
|CLNDBN=Generalized epilepsy with febrile seizures plus, type 2; Generalized epilepsy with febrile seizures plus, type 1
|Disease=Generalized epilepsy with febrile seizures plus; Generalized epilepsy with febrile seizures plus
|CLNACC=RCV000013746.16; RCV000059433.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1318:C1858673:604403:36387; NBK1318:C1858672:604233:36387
}}{{PMID Auto
|PMID=11254444
|Title=Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.
|OA=1
}}