rs1057516306

Orientation

plus

Stabilized

plus

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

Make rs1057516306(-;-)

Make rs1057516306(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

99891667

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs1057516306
dbSNP (classic)	rs1057516306
ClinGen	rs1057516306
ebi	rs1057516306
HLI	rs1057516306
Exac	rs1057516306
Gnomad	rs1057516306
Varsome	rs1057516306
LitVar	rs1057516306
Map	rs1057516306
PheGenI	rs1057516306
Biobank	rs1057516306
1000 genomes	rs1057516306
hgdp	rs1057516306
ensembl	rs1057516306
geneview	rs1057516306
scholar	rs1057516306
google	rs1057516306
pharmgkb	rs1057516306
gwascentral	rs1057516306
openSNP	rs1057516306
23andMe	rs1057516306
SNPshot	rs1057516306
SNPdbe	rs1057516306
MSV3d	rs1057516306
GWAS Ctlg	rs1057516306

Max Magnitude

0

ClinVar
Risk	rs1057516306(-;-)
Alt	rs1057516306(-;-)
Reference	Rs1057516306(C;C)
Significance	Probable-Pathogenic
Disease	Glycogen storage disease type III
Variation	info
Gene	AGL
CLNDBN	Glycogen storage disease type III
Reversed	0
HGVS	NC_000001.10:g.100357223delC
CLNSRC
CLNACC	RCV000410491.1,