{{Rsnum
|rsid=121918624
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCN1A
|position=166052882
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN1A
}}{{omim
|id=182389
|rsnum=121918624
|variant=0008
}}{{ClinVar
|rsid=121918624
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=166909392
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SCN1A:6323
|GENE_NAME=SCN1A
|GENE_ID=6323
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.166909392G>A
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=8831; 182389.0008
|CLNSIG=5
|CLNCUI=C0751122
|CLNDBN=Severe myoclonic epilepsy in infancy; not provided
|Disease=Severe myoclonic epilepsy in infancy; not provided
|CLNACC=RCV000032604.21; RCV000079595.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1318:C0751122:607208:33069:230437002
}}