{{Rsnum
|rsid=121917749
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCN2A
|position=165374700
|Gene_s=SCN2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=182390
|rsnum=121917749
|variant=0002
}}{{ClinVar
|rsid=121917749
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=166231210
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SCN2A:6326
|GENE_NAME=SCN2A
|GENE_ID=6326
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.166231210C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=182390.0002
|CLNSIG=5
|CLNCUI=C1843140
|CLNDBN=Benign familial neonatal-infantile seizures
|Disease=Benign familial neonatal-infantile seizures
|CLNACC=RCV000013736.21
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1843140:607745:140927:306
}}