rs104894166

Orientation

plus

Stabilized

plus

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

Make rs104894166(C;C)

Make rs104894166(C;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

93758280

Gene	LGI1, LOC101927013

is a	snp
is	mentioned by
dbSNP	rs104894166
dbSNP (classic)	rs104894166
ClinGen	rs104894166
ebi	rs104894166
HLI	rs104894166
Exac	rs104894166
Gnomad	rs104894166
Varsome	rs104894166
LitVar	rs104894166
Map	rs104894166
PheGenI	rs104894166
Biobank	rs104894166
1000 genomes	rs104894166
hgdp	rs104894166
ensembl	rs104894166
geneview	rs104894166
scholar	rs104894166
google	rs104894166
pharmgkb	rs104894166
gwascentral	rs104894166
openSNP	rs104894166
23andMe	rs104894166
SNPshot	rs104894166
SNPdbe	rs104894166
MSV3d	rs104894166
GWAS Ctlg	rs104894166

Max Magnitude

0

OMIM	604619
Desc
Variant	0004
Related	also

ClinVar
Risk	rs104894166(C;C)
Alt	rs104894166(C;C)
Reference	Rs104894166(T;T)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	LGI1 LOC101927013
CLNDBN	Epilepsy, lateral temporal lobe, autosomal dominant
Reversed	0
HGVS	NC_000010.10:g.95518037T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005766.3,