rs869025201

Orientation

plus

Stabilized

plus

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

Make rs869025201(C;C)

Make rs869025201(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

93797142

Gene

LGI1

is a	snp
is	mentioned by
dbSNP	rs869025201
dbSNP (classic)	rs869025201
ClinGen	rs869025201
ebi	rs869025201
HLI	rs869025201
Exac	rs869025201
Gnomad	rs869025201
Varsome	rs869025201
LitVar	rs869025201
Map	rs869025201
PheGenI	rs869025201
Biobank	rs869025201
1000 genomes	rs869025201
hgdp	rs869025201
ensembl	rs869025201
geneview	rs869025201
scholar	rs869025201
google	rs869025201
pharmgkb	rs869025201
gwascentral	rs869025201
openSNP	rs869025201
23andMe	rs869025201
SNPshot	rs869025201
SNPdbe	rs869025201
MSV3d	rs869025201
GWAS Ctlg	rs869025201

Max Magnitude

0

ClinVar
Risk	rs869025201(C;C)
Alt	rs869025201(C;C)
Reference	Rs869025201(T;T)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	LGI1
CLNDBN	Epilepsy, lateral temporal lobe, autosomal dominant
Reversed	0
HGVS	NC_000010.10:g.95556899T>C
CLNSRC
CLNACC	RCV000207482.1,