rs796065334

Orientation

minus

Stabilized

minus

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

Make rs796065334(-;G)

Make rs796065334(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

42929274

Gene

SLC2A1

is a	snp
is	mentioned by
dbSNP	rs796065334
dbSNP (classic)	rs796065334
ClinGen	rs796065334
ebi	rs796065334
HLI	rs796065334
Exac	rs796065334
Gnomad	rs796065334
Varsome	rs796065334
LitVar	rs796065334
Map	rs796065334
PheGenI	rs796065334
Biobank	rs796065334
1000 genomes	rs796065334
hgdp	rs796065334
ensembl	rs796065334
geneview	rs796065334
scholar	rs796065334
google	rs796065334
pharmgkb	rs796065334
gwascentral	rs796065334
openSNP	rs796065334
23andMe	rs796065334
SNPshot	rs796065334
SNPdbe	rs796065334
MSV3d	rs796065334
GWAS Ctlg	rs796065334

Max Magnitude

0

ClinVar
Risk	rs796065334(G;G)
Alt	rs796065334(G;G)
Reference	Rs796065334(-;-)
Significance	Pathogenic
Disease	GLUT1 deficiency syndrome 1 Epilepsy
Variation	info
Gene	SLC2A1
CLNDBN	GLUT1 deficiency syndrome 1 Epilepsy, idiopathic generalized, susceptibility to, 12
Reversed	1
HGVS	NC_000001.10:g.43394946dupC
CLNSRC
CLNACC	RCV000179917.1, RCV000179918.1,