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rs1057517405

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs1057517405(-;-)
Make rs1057517405(-;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99915402
GeneAGL
is asnp
is mentioned by
dbSNPrs1057517405
dbSNP (old)rs1057517405
ClinGenrs1057517405
ebirs1057517405
HLIrs1057517405
Exacrs1057517405
Gnomadrs1057517405
Varsomers1057517405
Maprs1057517405
PheGenIrs1057517405
Biobankrs1057517405
1000 genomesrs1057517405
hgdprs1057517405
ensemblrs1057517405
gopubmedrs1057517405
geneviewrs1057517405
scholarrs1057517405
googlers1057517405
pharmgkbrs1057517405
gwascentralrs1057517405
openSNPrs1057517405
23andMers1057517405
23andMe allrs1057517405
SNPshotrs1057517405
SNPdbers1057517405
MSV3drs1057517405
GWAS Ctlgrs1057517405
Max Magnitude0
ClinVar
Risk rs1057517405(-;-)
Alt rs1057517405(-;-)
Reference Rs1057517405(TT;TT)
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.100380958_100380959delTT
CLNSRC
CLNACC RCV000409452.1,