rs1060502054

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1060502054(C;T)

Make rs1060502054(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

93793200

Gene

LGI1

is a	snp
is	mentioned by
dbSNP	rs1060502054
dbSNP (classic)	rs1060502054
ClinGen	rs1060502054
ebi	rs1060502054
HLI	rs1060502054
Exac	rs1060502054
Gnomad	rs1060502054
Varsome	rs1060502054
LitVar	rs1060502054
Map	rs1060502054
PheGenI	rs1060502054
Biobank	rs1060502054
1000 genomes	rs1060502054
hgdp	rs1060502054
ensembl	rs1060502054
geneview	rs1060502054
scholar	rs1060502054
google	rs1060502054
pharmgkb	rs1060502054
gwascentral	rs1060502054
openSNP	rs1060502054
23andMe	rs1060502054
SNPshot	rs1060502054
SNPdbe	rs1060502054
MSV3d	rs1060502054
GWAS Ctlg	rs1060502054

Max Magnitude

0

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,