rs794729209

Orientation

plus

Stabilized

plus

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

Make rs794729209(A;A)

Make rs794729209(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

99875455

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs794729209
dbSNP (classic)	rs794729209
ClinGen	rs794729209
ebi	rs794729209
HLI	rs794729209
Exac	rs794729209
Gnomad	rs794729209
Varsome	rs794729209
LitVar	rs794729209
Map	rs794729209
PheGenI	rs794729209
Biobank	rs794729209
1000 genomes	rs794729209
hgdp	rs794729209
ensembl	rs794729209
geneview	rs794729209
scholar	rs794729209
google	rs794729209
pharmgkb	rs794729209
gwascentral	rs794729209
openSNP	rs794729209
23andMe	rs794729209
SNPshot	rs794729209
SNPdbe	rs794729209
MSV3d	rs794729209
GWAS Ctlg	rs794729209

Max Magnitude

0

ClinVar
Risk	rs794729209(A;A)
Alt	rs794729209(A;A)
Reference	Rs794729209(G;G)
Significance	Pathogenic
Disease	Glycogen storage disease type III
Variation	info
Gene	AGL
CLNDBN	Glycogen storage disease type III
Reversed	0
HGVS	NC_000001.10:g.100341011G>A
CLNSRC
CLNACC	RCV000184029.1,