rs1057516471

Orientation

plus

Stabilized

plus

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

Make rs1057516471(-;T)

Make rs1057516471(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

99870407

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs1057516471
dbSNP (classic)	rs1057516471
ClinGen	rs1057516471
ebi	rs1057516471
HLI	rs1057516471
Exac	rs1057516471
Gnomad	rs1057516471
Varsome	rs1057516471
LitVar	rs1057516471
Map	rs1057516471
PheGenI	rs1057516471
Biobank	rs1057516471
1000 genomes	rs1057516471
hgdp	rs1057516471
ensembl	rs1057516471
geneview	rs1057516471
scholar	rs1057516471
google	rs1057516471
pharmgkb	rs1057516471
gwascentral	rs1057516471
openSNP	rs1057516471
23andMe	rs1057516471
SNPshot	rs1057516471
SNPdbe	rs1057516471
MSV3d	rs1057516471
GWAS Ctlg	rs1057516471

Max Magnitude

0

ClinVar
Risk	rs1057516471(T;T)
Alt	rs1057516471(T;T)
Reference	Rs1057516471(-;-)
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.100335963dupT
CLNSRC
CLNACC	RCV000412273.1,