rs771961377

Orientation

plus

Stabilized

plus

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

Make rs771961377(C;T)

Make rs771961377(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

99861538

Gene

AGL

is a	snp
is	mentioned by
dbSNP	rs771961377
dbSNP (classic)	rs771961377
ClinGen	rs771961377
ebi	rs771961377
HLI	rs771961377
Exac	rs771961377
Gnomad	rs771961377
Varsome	rs771961377
LitVar	rs771961377
Map	rs771961377
PheGenI	rs771961377
Biobank	rs771961377
1000 genomes	rs771961377
hgdp	rs771961377
ensembl	rs771961377
geneview	rs771961377
scholar	rs771961377
google	rs771961377
pharmgkb	rs771961377
gwascentral	rs771961377
openSNP	rs771961377
23andMe	rs771961377
SNPshot	rs771961377
SNPdbe	rs771961377
MSV3d	rs771961377
GWAS Ctlg	rs771961377

Max Magnitude

0

ClinVar
Risk	rs771961377(T;T)
Alt	rs771961377(T;T)
Reference	Rs771961377(C;C)
Significance	Other
Disease	Glycogen storage disease type III
Variation	info
Gene	AGL
CLNDBN	Glycogen storage disease type III
Reversed	0
HGVS	NC_000001.10:g.100327094C>T
CLNSRC
CLNACC	RCV000169437.1,