Rs104894166

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Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894166(C;C)
Make rs104894166(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position93758280
GeneLGI1, LOC101927013
is asnp
is mentioned by
dbSNPrs104894166
PheGenIrs104894166
nextbiors104894166
hapmaprs104894166
1000 genomesrs104894166
hgdprs104894166
ensemblrs104894166
gopubmedrs104894166
geneviewrs104894166
scholarrs104894166
googlers104894166
pharmgkbrs104894166
gwascentralrs104894166
openSNPrs104894166
23andMers104894166
23andMe allrs104894166
SNP Nexus

SNPshotrs104894166
SNPdbers104894166
MSV3drs104894166
Max Magnitude0
OMIM604619
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894166(C;C)
Alt rs104894166(C;C)
Reference rs104894166(T;T)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95518037T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005766.1,