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rs1060502053

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502053(A;A)
Make rs1060502053(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position93797257
GeneLGI1
is asnp
is mentioned by
dbSNPrs1060502053
dbSNP (old)rs1060502053
ClinGenrs1060502053
ebirs1060502053
HLIrs1060502053
Exacrs1060502053
Gnomadrs1060502053
Varsomers1060502053
Maprs1060502053
PheGenIrs1060502053
Biobankrs1060502053
1000 genomesrs1060502053
hgdprs1060502053
ensemblrs1060502053
gopubmedrs1060502053
geneviewrs1060502053
scholarrs1060502053
googlers1060502053
pharmgkbrs1060502053
gwascentralrs1060502053
openSNPrs1060502053
23andMers1060502053
23andMe allrs1060502053
SNPshotrs1060502053
SNPdbers1060502053
MSV3drs1060502053
GWAS Ctlgrs1060502053
Max Magnitude0
ClinVar
Risk rs1060502053(A;A)
Alt rs1060502053(A;A)
Reference Rs1060502053(G;G)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95557014G>A
CLNSRC
CLNACC RCV000468265.1,