rs1057516803

Orientation

plus

Stabilized

plus

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

Make rs1057516803(-;A)

Make rs1057516803(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

99912479

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs1057516803
dbSNP (classic)	rs1057516803
ClinGen	rs1057516803
ebi	rs1057516803
HLI	rs1057516803
Exac	rs1057516803
Gnomad	rs1057516803
Varsome	rs1057516803
LitVar	rs1057516803
Map	rs1057516803
PheGenI	rs1057516803
Biobank	rs1057516803
1000 genomes	rs1057516803
hgdp	rs1057516803
ensembl	rs1057516803
geneview	rs1057516803
scholar	rs1057516803
google	rs1057516803
pharmgkb	rs1057516803
gwascentral	rs1057516803
openSNP	rs1057516803
23andMe	rs1057516803
SNPshot	rs1057516803
SNPdbe	rs1057516803
MSV3d	rs1057516803
GWAS Ctlg	rs1057516803

Max Magnitude

0

ClinVar
Risk	rs1057516803(A;A)
Alt	rs1057516803(A;A)
Reference	Rs1057516803(-;-)
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.100378035dupA
CLNSRC
CLNACC	RCV000412031.1,