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rs28937874

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28937874(A;C)
Make rs28937874(C;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position93797277
GeneLGI1
is asnp
is mentioned by
dbSNPrs28937874
ebirs28937874
HLIrs28937874
Exacrs28937874
Varsomers28937874
Maprs28937874
PheGenIrs28937874
hapmaprs28937874
1000 genomesrs28937874
hgdprs28937874
ensemblrs28937874
gopubmedrs28937874
geneviewrs28937874
scholarrs28937874
googlers28937874
pharmgkbrs28937874
gwascentralrs28937874
openSNPrs28937874
23andMers28937874
23andMe allrs28937874
SNP Nexus

SNPshotrs28937874
SNPdbers28937874
MSV3drs28937874
GWAS Ctlgrs28937874
Max Magnitude0
OMIM604619
DescEPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT
Variant0001
Relatedalso
Neighborrs28939075
Distance195


ClinVar
Risk rs28937874(C;C)
Alt rs28937874(C;C)
Reference rs28937874(A;A)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95557034A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005763.2,