rs80359832

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(CTC;CTC)	0	common in clinvar
(I;I)	0	common genotype

Make rs80359832(-;-)

Make rs80359832(-;CTC)

Reference

GRCh38 38.1/141

Chromosome

1

Position

42930635

Gene

SLC2A1

is a	snp
is	mentioned by
dbSNP	rs80359832
dbSNP (classic)	rs80359832
ClinGen	rs80359832
ebi	rs80359832
HLI	rs80359832
Exac	rs80359832
Gnomad	rs80359832
Varsome	rs80359832
LitVar	rs80359832
Map	rs80359832
PheGenI	rs80359832
Biobank	rs80359832
1000 genomes	rs80359832
hgdp	rs80359832
ensembl	rs80359832
geneview	rs80359832
scholar	rs80359832
google	rs80359832
pharmgkb	rs80359832
gwascentral	rs80359832
openSNP	rs80359832
23andMe	rs80359832
SNPshot	rs80359832
SNPdbe	rs80359832
MSV3d	rs80359832
GWAS Ctlg	rs80359832

Max Magnitude

0

ClinVar
Risk	rs80359832(-;-)
Alt	rs80359832(-;-)
Reference	Rs80359832(CTC;CTC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SLC2A1
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.43396306_43396308delGAG
CLNSRC
CLNACC	RCV000478031.1,

[PMID 15622525] Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.