{{Rsnum
|rsid=387906687
|Chromosome=2
|position=165310379
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN2A
|Gene_s=SCN2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=2
|CLNACC=RCV000022770.16
|CLNALLE=1
|CLNDBN=Benign familial neonatal-infantile seizures
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1843140:607745:140927:306
|CLNHGVS=NC_000002.11:g.166166889A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=182390.0012
|Disease=Benign familial neonatal-infantile seizures
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=166166889
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906687
|GENEINFO=SCN2A:6326
|GENE_ID=6326
|GENE_NAME=SCN2A
}}