rs28939075

Orientation

plus

Stabilized

plus

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

Make rs28939075(G;G)

Make rs28939075(G;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

93797082

Gene

LGI1

is a	snp
is	mentioned by
dbSNP	rs28939075
dbSNP (classic)	rs28939075
ClinGen	rs28939075
ebi	rs28939075
HLI	rs28939075
Exac	rs28939075
Gnomad	rs28939075
Varsome	rs28939075
LitVar	rs28939075
Map	rs28939075
PheGenI	rs28939075
Biobank	rs28939075
1000 genomes	rs28939075
hgdp	rs28939075
ensembl	rs28939075
geneview	rs28939075
scholar	rs28939075
google	rs28939075
pharmgkb	rs28939075
gwascentral	rs28939075
openSNP	rs28939075
23andMe	rs28939075
SNPshot	rs28939075
SNPdbe	rs28939075
MSV3d	rs28939075
GWAS Ctlg	rs28939075

Max Magnitude

0

OMIM	604619
Desc	EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT
Variant	0007
Related	also

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 UniProtKB (protein)
CLNACC	RCV000005768.3,