rs28937874

Orientation

plus

Stabilized

plus

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

Make rs28937874(A;C)

Make rs28937874(C;C)

Reference

GRCh38 38.1/141

Chromosome

10

Position

93797277

Gene

LGI1

is a	snp
is	mentioned by
dbSNP	rs28937874
dbSNP (classic)	rs28937874
ClinGen	rs28937874
ebi	rs28937874
HLI	rs28937874
Exac	rs28937874
Gnomad	rs28937874
Varsome	rs28937874
LitVar	rs28937874
Map	rs28937874
PheGenI	rs28937874
Biobank	rs28937874
1000 genomes	rs28937874
hgdp	rs28937874
ensembl	rs28937874
geneview	rs28937874
scholar	rs28937874
google	rs28937874
pharmgkb	rs28937874
gwascentral	rs28937874
openSNP	rs28937874
23andMe	rs28937874
SNPshot	rs28937874
SNPdbe	rs28937874
MSV3d	rs28937874
GWAS Ctlg	rs28937874

Max Magnitude

0

OMIM	604619
Desc	EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT
Variant	0001
Related	also

ClinVar
Risk	rs28937874(C;C)
Alt	rs28937874(C;C)
Reference	Rs28937874(A;A)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	LGI1
CLNDBN	Epilepsy, lateral temporal lobe, autosomal dominant
Reversed	0
HGVS	NC_000010.10:g.95557034A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005763.2,