{{Rsnum
|rsid=104894166
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LGI1
|position=93758280
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LGI1,LOC101927013
}}{{omim
|id=604619
|rsnum=104894166
|variant=0004
}}{{ClinVar
|rsid=104894166
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=95518037
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=LGI1:9211
|GENE_NAME=LGI1
|GENE_ID=9211
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.95518037T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604619.0004; 604619.0006
|CLNSIG=5
|CLNCUI=C1838062
|CLNDBN=Epilepsy, lateral temporal lobe, autosomal dominant
|Disease=Epilepsy
|CLNACC=RCV000005766.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1537:C1838062:600512
}}