Rs104894167

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Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894167(C;C)
Make rs104894167(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position93793207
GeneLGI1
is asnp
is mentioned by
dbSNPrs104894167
PheGenIrs104894167
nextbiors104894167
hapmaprs104894167
1000 genomesrs104894167
hgdprs104894167
ensemblrs104894167
gopubmedrs104894167
geneviewrs104894167
scholarrs104894167
googlers104894167
pharmgkbrs104894167
gwascentralrs104894167
openSNPrs104894167
23andMers104894167
23andMe allrs104894167
SNP Nexus

SNPshotrs104894167
SNPdbers104894167
MSV3drs104894167
Max Magnitude0
OMIM604619
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104894167(C;C)
Alt rs104894167(C;C)
Reference rs104894167(T;T)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95552964T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005770.1,