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rs119488099

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119488099(C;T)
Make rs119488099(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position93777592
GeneLGI1
is asnp
is mentioned by
dbSNPrs119488099
ebirs119488099
HLIrs119488099
Exacrs119488099
Varsomers119488099
Maprs119488099
PheGenIrs119488099
hapmaprs119488099
1000 genomesrs119488099
hgdprs119488099
ensemblrs119488099
gopubmedrs119488099
geneviewrs119488099
scholarrs119488099
googlers119488099
pharmgkbrs119488099
gwascentralrs119488099
openSNPrs119488099
23andMers119488099
23andMe allrs119488099
SNP Nexus

SNPshotrs119488099
SNPdbers119488099
MSV3drs119488099
GWAS Ctlgrs119488099
Max Magnitude0
OMIM604619
Desc
Variant0010
Relatedalso
ClinVar
Risk rs119488099(T;T)
Alt rs119488099(T;T)
Reference rs119488099(C;C)
Significance Pathogenic
Disease Epilepsy not provided
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant not provided
Reversed 0
HGVS NC_000010.10:g.95537349C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005771.2, RCV000188042.1,