rs786204655

Orientation

plus

Stabilized

plus

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

Make rs786204655(-;A)

Make rs786204655(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

99915448

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs786204655
dbSNP (classic)	rs786204655
ClinGen	rs786204655
ebi	rs786204655
HLI	rs786204655
Exac	rs786204655
Gnomad	rs786204655
Varsome	rs786204655
LitVar	rs786204655
Map	rs786204655
PheGenI	rs786204655
Biobank	rs786204655
1000 genomes	rs786204655
hgdp	rs786204655
ensembl	rs786204655
geneview	rs786204655
scholar	rs786204655
google	rs786204655
pharmgkb	rs786204655
gwascentral	rs786204655
openSNP	rs786204655
23andMe	rs786204655
SNPshot	rs786204655
SNPdbe	rs786204655
MSV3d	rs786204655
GWAS Ctlg	rs786204655

Max Magnitude

0

ClinVar
Risk	rs786204655(A;A)
Alt	rs786204655(A;A)
Reference	Rs786204655(-;-)
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.100381004dupA
CLNSRC
CLNACC	RCV000169447.1,