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rs869025201

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025201(C;C)
Make rs869025201(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position93797142
GeneLGI1
is asnp
is mentioned by
dbSNPrs869025201
ebirs869025201
HLIrs869025201
Exacrs869025201
Varsomers869025201
Maprs869025201
PheGenIrs869025201
hapmaprs869025201
1000 genomesrs869025201
hgdprs869025201
ensemblrs869025201
gopubmedrs869025201
geneviewrs869025201
scholarrs869025201
googlers869025201
pharmgkbrs869025201
gwascentralrs869025201
openSNPrs869025201
23andMers869025201
23andMe allrs869025201
SNP Nexus

SNPshotrs869025201
SNPdbers869025201
MSV3drs869025201
GWAS Ctlgrs869025201
Max Magnitude0
ClinVar
Risk rs869025201(C;C)
Alt rs869025201(C;C)
Reference rs869025201(T;T)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95556899T>C
CLNSRC
CLNACC RCV000207482.1,