Have questions? Visit https://www.reddit.com/r/SNPedia

rs28939075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28939075(G;G)
Make rs28939075(G;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position93797082
GeneLGI1
is asnp
is mentioned by
dbSNPrs28939075
ebirs28939075
HLIrs28939075
Exacrs28939075
Varsomers28939075
Maprs28939075
PheGenIrs28939075
hapmaprs28939075
1000 genomesrs28939075
hgdprs28939075
ensemblrs28939075
gopubmedrs28939075
geneviewrs28939075
scholarrs28939075
googlers28939075
pharmgkbrs28939075
gwascentralrs28939075
openSNPrs28939075
23andMers28939075
23andMe allrs28939075
SNP Nexus

SNPshotrs28939075
SNPdbers28939075
MSV3drs28939075
GWAS Ctlgrs28939075
Max Magnitude0
OMIM604619
DescEPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT
Variant0007
Relatedalso
Neighborrs28937874
Distance195


ClinVar
Risk rs28939075(G;G)
Alt rs28939075(G;G)
Reference rs28939075(T;T)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95556839T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005768.2,