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rs797044999

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044999(C;T)
Make rs797044999(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93797547
GeneLGI1
is asnp
is mentioned by
dbSNPrs797044999
ebirs797044999
HLIrs797044999
Exacrs797044999
Varsomers797044999
Maprs797044999
PheGenIrs797044999
hapmaprs797044999
1000 genomesrs797044999
hgdprs797044999
ensemblrs797044999
gopubmedrs797044999
geneviewrs797044999
scholarrs797044999
googlers797044999
pharmgkbrs797044999
gwascentralrs797044999
openSNPrs797044999
23andMers797044999
23andMe allrs797044999
SNP Nexus

SNPshotrs797044999
SNPdbers797044999
MSV3drs797044999
GWAS Ctlgrs797044999
Max Magnitude0
ClinVar
Risk rs797044999(T;T)
Alt rs797044999(T;T)
Reference rs797044999(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95557304C>T
CLNSRC
CLNACC RCV000192478.1,