rs794727051

Orientation

plus

Stabilized

plus

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

Make rs794727051(-;-)

Make rs794727051(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

99877702

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs794727051
dbSNP (classic)	rs794727051
ClinGen	rs794727051
ebi	rs794727051
HLI	rs794727051
Exac	rs794727051
Gnomad	rs794727051
Varsome	rs794727051
LitVar	rs794727051
Map	rs794727051
PheGenI	rs794727051
Biobank	rs794727051
1000 genomes	rs794727051
hgdp	rs794727051
ensembl	rs794727051
geneview	rs794727051
scholar	rs794727051
google	rs794727051
pharmgkb	rs794727051
gwascentral	rs794727051
openSNP	rs794727051
23andMe	rs794727051
SNPshot	rs794727051
SNPdbe	rs794727051
MSV3d	rs794727051
GWAS Ctlg	rs794727051

Max Magnitude

0

ClinVar
Risk	rs794727051(-;-)
Alt	rs794727051(-;-)
Reference	Rs794727051(T;T)
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.100343258delT
CLNSRC
CLNACC	RCV000174259.1,