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rs1057517079

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517079(-;A)
Make rs1057517079(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99900716
GeneAGL
is asnp
is mentioned by
dbSNPrs1057517079
dbSNP (old)rs1057517079
ClinGenrs1057517079
ebirs1057517079
HLIrs1057517079
Exacrs1057517079
Gnomadrs1057517079
Varsomers1057517079
Maprs1057517079
PheGenIrs1057517079
Biobankrs1057517079
1000 genomesrs1057517079
hgdprs1057517079
ensemblrs1057517079
gopubmedrs1057517079
geneviewrs1057517079
scholarrs1057517079
googlers1057517079
pharmgkbrs1057517079
gwascentralrs1057517079
openSNPrs1057517079
23andMers1057517079
23andMe allrs1057517079
SNPshotrs1057517079
SNPdbers1057517079
MSV3drs1057517079
GWAS Ctlgrs1057517079
Max Magnitude0
ClinVar
Risk rs1057517079(A;A)
Alt rs1057517079(A;A)
Reference Rs1057517079(-;-)
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.100366272dupA
CLNSRC
CLNACC RCV000410096.1,