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rs1057517136

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517136(-;-)
Make rs1057517136(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99881661
GeneAGL
is asnp
is mentioned by
dbSNPrs1057517136
dbSNP (old)rs1057517136
ClinGenrs1057517136
ebirs1057517136
HLIrs1057517136
Exacrs1057517136
Gnomadrs1057517136
Varsomers1057517136
Maprs1057517136
PheGenIrs1057517136
Biobankrs1057517136
1000 genomesrs1057517136
hgdprs1057517136
ensemblrs1057517136
gopubmedrs1057517136
geneviewrs1057517136
scholarrs1057517136
googlers1057517136
pharmgkbrs1057517136
gwascentralrs1057517136
openSNPrs1057517136
23andMers1057517136
23andMe allrs1057517136
SNPshotrs1057517136
SNPdbers1057517136
MSV3drs1057517136
GWAS Ctlgrs1057517136
Max Magnitude0
ClinVar
Risk rs1057517136(-;-)
Alt rs1057517136(-;-)
Reference Rs1057517136(A;A)
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.100347217delA
CLNSRC
CLNACC RCV000409251.1,