rs1057517136

Orientation

plus

Stabilized

plus

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

Make rs1057517136(-;-)

Make rs1057517136(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

99881661

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs1057517136
dbSNP (classic)	rs1057517136
ClinGen	rs1057517136
ebi	rs1057517136
HLI	rs1057517136
Exac	rs1057517136
Gnomad	rs1057517136
Varsome	rs1057517136
LitVar	rs1057517136
Map	rs1057517136
PheGenI	rs1057517136
Biobank	rs1057517136
1000 genomes	rs1057517136
hgdp	rs1057517136
ensembl	rs1057517136
geneview	rs1057517136
scholar	rs1057517136
google	rs1057517136
pharmgkb	rs1057517136
gwascentral	rs1057517136
openSNP	rs1057517136
23andMe	rs1057517136
SNPshot	rs1057517136
SNPdbe	rs1057517136
MSV3d	rs1057517136
GWAS Ctlg	rs1057517136

Max Magnitude

0

ClinVar
Risk	rs1057517136(-;-)
Alt	rs1057517136(-;-)
Reference	Rs1057517136(A;A)
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.100347217delA
CLNSRC
CLNACC	RCV000409251.1,