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rs1057516803

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516803(-;A)
Make rs1057516803(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99912479
GeneAGL
is asnp
is mentioned by
dbSNPrs1057516803
dbSNP (classic)rs1057516803
ClinGenrs1057516803
ebirs1057516803
HLIrs1057516803
Exacrs1057516803
Gnomadrs1057516803
Varsomers1057516803
LitVarrs1057516803
Maprs1057516803
PheGenIrs1057516803
Biobankrs1057516803
1000 genomesrs1057516803
hgdprs1057516803
ensemblrs1057516803
geneviewrs1057516803
scholarrs1057516803
googlers1057516803
pharmgkbrs1057516803
gwascentralrs1057516803
openSNPrs1057516803
23andMers1057516803
23andMe allrs1057516803
SNPshotrs1057516803
SNPdbers1057516803
MSV3drs1057516803
GWAS Ctlgrs1057516803
Max Magnitude0
ClinVar
Risk rs1057516803(A;A)
Alt rs1057516803(A;A)
Reference Rs1057516803(-;-)
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.100378035dupA
CLNSRC
CLNACC RCV000412031.1,