rs794727255

Merged into

rs113994127

Orientation

plus

Stabilized

plus

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

Make rs794727255(-;-)

Make rs794727255(-;GA)

Make rs794727255(GA;GA)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

99851060

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs794727255
dbSNP (classic)	rs794727255
ClinGen	rs794727255
ebi	rs794727255
HLI	rs794727255
Exac	rs794727255
Gnomad	rs794727255
Varsome	rs794727255
LitVar	rs794727255
Map	rs794727255
PheGenI	rs794727255
Biobank	rs794727255
1000 genomes	rs794727255
hgdp	rs794727255
ensembl	rs794727255
geneview	rs794727255
scholar	rs794727255
google	rs794727255
pharmgkb	rs794727255
gwascentral	rs794727255
openSNP	rs794727255
23andMe	rs794727255
SNPshot	rs794727255
SNPdbe	rs794727255
MSV3d	rs794727255
GWAS Ctlg	rs794727255

Status

Merged into rs113994127

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs794727255(AG;AG)
Significance	Pathogenic
Disease	Glycogen storage disease IIIb Glycogen storage disease type III
Variation	info
Gene	AGL
CLNDBN	Glycogen storage disease IIIb Glycogen storage disease type III
Reversed	0
HGVS	NC_000001.10:g.100316616_100316617delGA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001155.3, RCV000175637.2,