Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057516984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516984(-;T)
Make rs1057516984(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99884443
GeneAGL
is asnp
is mentioned by
dbSNPrs1057516984
dbSNP (classic)rs1057516984
ClinGenrs1057516984
ebirs1057516984
HLIrs1057516984
Exacrs1057516984
Gnomadrs1057516984
Varsomers1057516984
LitVarrs1057516984
Maprs1057516984
PheGenIrs1057516984
Biobankrs1057516984
1000 genomesrs1057516984
hgdprs1057516984
ensemblrs1057516984
geneviewrs1057516984
scholarrs1057516984
googlers1057516984
pharmgkbrs1057516984
gwascentralrs1057516984
openSNPrs1057516984
23andMers1057516984
23andMe allrs1057516984
SNPshotrs1057516984
SNPdbers1057516984
MSV3drs1057516984
GWAS Ctlgrs1057516984
Max Magnitude0
ClinVar
Risk rs1057516984(T;T)
Alt rs1057516984(T;T)
Reference Rs1057516984(-;-)
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.100349999dupT
CLNSRC
CLNACC RCV000412255.1,