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rs797044998

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044998(C;T)
Make rs797044998(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93797549
GeneLGI1
is asnp
is mentioned by
dbSNPrs797044998
ebirs797044998
HLIrs797044998
Exacrs797044998
Varsomers797044998
Maprs797044998
PheGenIrs797044998
hapmaprs797044998
1000 genomesrs797044998
hgdprs797044998
ensemblrs797044998
gopubmedrs797044998
geneviewrs797044998
scholarrs797044998
googlers797044998
pharmgkbrs797044998
gwascentralrs797044998
openSNPrs797044998
23andMers797044998
23andMe allrs797044998
SNP Nexus

SNPshotrs797044998
SNPdbers797044998
MSV3drs797044998
GWAS Ctlgrs797044998
Max Magnitude0
ClinVar
Risk rs797044998(T;T)
Alt rs797044998(T;T)
Reference rs797044998(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95557306C>T
CLNSRC
CLNACC RCV000193378.1,