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rs1060502054

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502054(C;T)
Make rs1060502054(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position93793200
GeneLGI1
is asnp
is mentioned by
dbSNPrs1060502054
dbSNP (old)rs1060502054
ClinGenrs1060502054
ebirs1060502054
HLIrs1060502054
Exacrs1060502054
Gnomadrs1060502054
Varsomers1060502054
Maprs1060502054
PheGenIrs1060502054
Biobankrs1060502054
1000 genomesrs1060502054
hgdprs1060502054
ensemblrs1060502054
gopubmedrs1060502054
geneviewrs1060502054
scholarrs1060502054
googlers1060502054
pharmgkbrs1060502054
gwascentralrs1060502054
openSNPrs1060502054
23andMers1060502054
23andMe allrs1060502054
SNPshotrs1060502054
SNPdbers1060502054
MSV3drs1060502054
GWAS Ctlgrs1060502054
Max Magnitude0
ClinVar
Risk rs1060502054(T;T)
Alt rs1060502054(T;T)
Reference Rs1060502054(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95552957C>T
CLNSRC
CLNACC RCV000460385.1,