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rs1057517425

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517425(-;-)
Make rs1057517425(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99884430
GeneAGL
is asnp
is mentioned by
dbSNPrs1057517425
dbSNP (old)rs1057517425
ClinGenrs1057517425
ebirs1057517425
HLIrs1057517425
Exacrs1057517425
Gnomadrs1057517425
Varsomers1057517425
Maprs1057517425
PheGenIrs1057517425
Biobankrs1057517425
1000 genomesrs1057517425
hgdprs1057517425
ensemblrs1057517425
gopubmedrs1057517425
geneviewrs1057517425
scholarrs1057517425
googlers1057517425
pharmgkbrs1057517425
gwascentralrs1057517425
openSNPrs1057517425
23andMers1057517425
23andMe allrs1057517425
SNPshotrs1057517425
SNPdbers1057517425
MSV3drs1057517425
GWAS Ctlgrs1057517425
Max Magnitude0
ClinVar
Risk rs1057517425(-;-)
Alt rs1057517425(-;-)
Reference Rs1057517425(C;C)
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.100349986delC
CLNSRC
CLNACC RCV000409805.1,