rs267606639

Orientation

plus

Stabilized

plus

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

Make rs267606639(A;G)

Make rs267606639(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

99900712

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs267606639
dbSNP (classic)	rs267606639
ClinGen	rs267606639
ebi	rs267606639
HLI	rs267606639
Exac	rs267606639
Gnomad	rs267606639
Varsome	rs267606639
LitVar	rs267606639
Map	rs267606639
PheGenI	rs267606639
Biobank	rs267606639
1000 genomes	rs267606639
hgdp	rs267606639
ensembl	rs267606639
geneview	rs267606639
scholar	rs267606639
google	rs267606639
pharmgkb	rs267606639
gwascentral	rs267606639
openSNP	rs267606639
23andMe	rs267606639
SNPshot	rs267606639
SNPdbe	rs267606639
MSV3d	rs267606639
GWAS Ctlg	rs267606639

Max Magnitude

0

ClinVar
Risk	rs267606639(G;G)
Alt	rs267606639(G;G)
Reference	Rs267606639(A;A)
Significance	Pathogenic
Disease	Glycogen storage disease IIIc
Variation	info
Gene	AGL
CLNDBN	Glycogen storage disease IIIc
Reversed	0
HGVS	NC_000001.10:g.100366268A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001166.3,