rs1057516666

Orientation

plus

Stabilized

plus

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

Make rs1057516666(-;-)

Make rs1057516666(-;GT)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

99881301

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs1057516666
dbSNP (classic)	rs1057516666
ClinGen	rs1057516666
ebi	rs1057516666
HLI	rs1057516666
Exac	rs1057516666
Gnomad	rs1057516666
Varsome	rs1057516666
LitVar	rs1057516666
Map	rs1057516666
PheGenI	rs1057516666
Biobank	rs1057516666
1000 genomes	rs1057516666
hgdp	rs1057516666
ensembl	rs1057516666
geneview	rs1057516666
scholar	rs1057516666
google	rs1057516666
pharmgkb	rs1057516666
gwascentral	rs1057516666
openSNP	rs1057516666
23andMe	rs1057516666
SNPshot	rs1057516666
SNPdbe	rs1057516666
MSV3d	rs1057516666
GWAS Ctlg	rs1057516666

Max Magnitude

0

ClinVar
Risk	rs1057516666(-;-)
Alt	rs1057516666(-;-)
Reference	Rs1057516666(GT;GT)
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.100346857_100346858delGT
CLNSRC
CLNACC	RCV000410044.1,