rs786204678

Orientation

plus

Stabilized

plus

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

Make rs786204678(-;-)

Make rs786204678(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

99876558

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs786204678
dbSNP (classic)	rs786204678
ClinGen	rs786204678
ebi	rs786204678
HLI	rs786204678
Exac	rs786204678
Gnomad	rs786204678
Varsome	rs786204678
LitVar	rs786204678
Map	rs786204678
PheGenI	rs786204678
Biobank	rs786204678
1000 genomes	rs786204678
hgdp	rs786204678
ensembl	rs786204678
geneview	rs786204678
scholar	rs786204678
google	rs786204678
pharmgkb	rs786204678
gwascentral	rs786204678
openSNP	rs786204678
23andMe	rs786204678
SNPshot	rs786204678
SNPdbe	rs786204678
MSV3d	rs786204678
GWAS Ctlg	rs786204678

Max Magnitude

0

ClinVar
Risk	rs786204678(-;-)
Alt	rs786204678(-;-)
Reference	Rs786204678(G;G)
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.100342114delG
CLNSRC
CLNACC	RCV000169486.1,