{{Rsnum
|rsid=104894718
|Gene=SCN1B
|Chromosome=19
|position=35033654
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=SCN1B
}}{{omim
|id=600235
|rsnum=104894718
|variant=0001
}}{{ClinVar
|rsid=104894718
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=35524558
|CHROM=19
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|GENEINFO=SCN1B:6324
|GENE_NAME=SCN1B
|GENE_ID=6324
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.35524558C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600235.0001
|CLNSIG=5
|CLNCUI=C1858672
|CLNDBN=Generalized epilepsy with febrile seizures plus, type 1; Generalized epilepsy with febrile seizures plus
|Disease=Generalized epilepsy with febrile seizures plus; Generalized epilepsy with febrile seizures plus
|CLNACC=RCV000009834.4; RCV000030434.1
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1318:C1858672:604233:36387; C3502809
|COMMON=0
}}