{{Rsnum
|rsid=121917918
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN1A
|position=166058651
|Gene_s=SCN1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=2
|CLNACC=RCV000059400.1; RCV000079571.1
|CLNALLE=1
|CLNDBN=Severe myoclonic epilepsy in infancy; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1318:C0751122:607208:33069:230437002
|CLNHGVS=NC_000002.11:g.166915161C>T
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=Emory University; UniProtKB (variants)
|CLNSRCID=7632; VAR_029661
|Disease=Severe myoclonic epilepsy in infancy; not provided
|FwdALT=A
|FwdREF=G
|GENEINFO=SCN1A:6323
|GENE_ID=6323
|GENE_NAME=SCN1A
|REF=C
|RSPOS=166915161
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=121917918
}}