rs1057517017

Orientation

plus

Stabilized

plus

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

Make rs1057517017(-;T)

Make rs1057517017(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

99910818

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs1057517017
dbSNP (classic)	rs1057517017
ClinGen	rs1057517017
ebi	rs1057517017
HLI	rs1057517017
Exac	rs1057517017
Gnomad	rs1057517017
Varsome	rs1057517017
LitVar	rs1057517017
Map	rs1057517017
PheGenI	rs1057517017
Biobank	rs1057517017
1000 genomes	rs1057517017
hgdp	rs1057517017
ensembl	rs1057517017
geneview	rs1057517017
scholar	rs1057517017
google	rs1057517017
pharmgkb	rs1057517017
gwascentral	rs1057517017
openSNP	rs1057517017
23andMe	rs1057517017
SNPshot	rs1057517017
SNPdbe	rs1057517017
MSV3d	rs1057517017
GWAS Ctlg	rs1057517017

Max Magnitude

0

ClinVar
Risk	rs1057517017(T;T)
Alt	rs1057517017(T;T)
Reference	Rs1057517017(-;-)
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.100376374dupT
CLNSRC
CLNACC	RCV000410845.1,