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rs1057516306

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516306(-;-)
Make rs1057516306(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99891667
GeneAGL
is asnp
is mentioned by
dbSNPrs1057516306
dbSNP (old)rs1057516306
ClinGenrs1057516306
ebirs1057516306
HLIrs1057516306
Exacrs1057516306
Gnomadrs1057516306
Varsomers1057516306
Maprs1057516306
PheGenIrs1057516306
Biobankrs1057516306
1000 genomesrs1057516306
hgdprs1057516306
ensemblrs1057516306
gopubmedrs1057516306
geneviewrs1057516306
scholarrs1057516306
googlers1057516306
pharmgkbrs1057516306
gwascentralrs1057516306
openSNPrs1057516306
23andMers1057516306
23andMe allrs1057516306
SNPshotrs1057516306
SNPdbers1057516306
MSV3drs1057516306
GWAS Ctlgrs1057516306
Max Magnitude0
ClinVar
Risk rs1057516306(-;-)
Alt rs1057516306(-;-)
Reference Rs1057516306(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.100357223delC
CLNSRC
CLNACC RCV000410491.1,