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rs1057517017

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517017(-;T)
Make rs1057517017(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99910818
GeneAGL
is asnp
is mentioned by
dbSNPrs1057517017
dbSNP (old)rs1057517017
ClinGenrs1057517017
ebirs1057517017
HLIrs1057517017
Exacrs1057517017
Gnomadrs1057517017
Varsomers1057517017
Maprs1057517017
PheGenIrs1057517017
Biobankrs1057517017
1000 genomesrs1057517017
hgdprs1057517017
ensemblrs1057517017
gopubmedrs1057517017
geneviewrs1057517017
scholarrs1057517017
googlers1057517017
pharmgkbrs1057517017
gwascentralrs1057517017
openSNPrs1057517017
23andMers1057517017
23andMe allrs1057517017
SNPshotrs1057517017
SNPdbers1057517017
MSV3drs1057517017
GWAS Ctlgrs1057517017
Max Magnitude0
ClinVar
Risk rs1057517017(T;T)
Alt rs1057517017(T;T)
Reference Rs1057517017(-;-)
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.100376374dupT
CLNSRC
CLNACC RCV000410845.1,