rs113994134

Orientation

plus

Stabilized

plus

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

Make rs113994134(-;-)

Make rs113994134(-;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

99916705

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs113994134
dbSNP (classic)	rs113994134
ClinGen	rs113994134
ebi	rs113994134
HLI	rs113994134
Exac	rs113994134
Gnomad	rs113994134
Varsome	rs113994134
LitVar	rs113994134
Map	rs113994134
PheGenI	rs113994134
Biobank	rs113994134
1000 genomes	rs113994134
hgdp	rs113994134
ensembl	rs113994134
geneview	rs113994134
scholar	rs113994134
google	rs113994134
pharmgkb	rs113994134
gwascentral	rs113994134
openSNP	rs113994134
23andMe	rs113994134
SNPshot	rs113994134
SNPdbe	rs113994134
MSV3d	rs113994134
GWAS Ctlg	rs113994134

Merged from

Rs387906245

Max Magnitude

0

ClinVar
Risk	rs113994134(-;-)
Alt	rs113994134(-;-)
Reference	Rs113994134(T;T)
Significance	Pathogenic
Disease	Glycogen storage disease IIIa Glycogen storage disease type III
Variation	info
Gene	AGL
CLNDBN	Glycogen storage disease IIIa Glycogen storage disease type III
Reversed	0
HGVS	NC_000001.10:g.100382262delT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001156.3, RCV000177731.2,

OMIM	232400
Desc
Variant
Related	also