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rs1057516937

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1057516937(-;-)
Make rs1057516937(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99910827
GeneAGL
is asnp
is mentioned by
dbSNPrs1057516937
dbSNP (old)rs1057516937
ClinGenrs1057516937
ebirs1057516937
HLIrs1057516937
Exacrs1057516937
Gnomadrs1057516937
Varsomers1057516937
Maprs1057516937
PheGenIrs1057516937
Biobankrs1057516937
1000 genomesrs1057516937
hgdprs1057516937
ensemblrs1057516937
gopubmedrs1057516937
geneviewrs1057516937
scholarrs1057516937
googlers1057516937
pharmgkbrs1057516937
gwascentralrs1057516937
openSNPrs1057516937
23andMers1057516937
23andMe allrs1057516937
SNPshotrs1057516937
SNPdbers1057516937
MSV3drs1057516937
GWAS Ctlgrs1057516937
Max Magnitude0
ClinVar
Risk rs1057516937(-;-)
Alt rs1057516937(-;-)
Reference Rs1057516937(AG;AG)
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.100376383_100376384delAG
CLNSRC
CLNACC RCV000410186.1,