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rs1057516666

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs1057516666(-;-)
Make rs1057516666(-;GT)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99881301
GeneAGL
is asnp
is mentioned by
dbSNPrs1057516666
dbSNP (old)rs1057516666
ClinGenrs1057516666
ebirs1057516666
HLIrs1057516666
Exacrs1057516666
Gnomadrs1057516666
Varsomers1057516666
Maprs1057516666
PheGenIrs1057516666
Biobankrs1057516666
1000 genomesrs1057516666
hgdprs1057516666
ensemblrs1057516666
gopubmedrs1057516666
geneviewrs1057516666
scholarrs1057516666
googlers1057516666
pharmgkbrs1057516666
gwascentralrs1057516666
openSNPrs1057516666
23andMers1057516666
23andMe allrs1057516666
SNPshotrs1057516666
SNPdbers1057516666
MSV3drs1057516666
GWAS Ctlgrs1057516666
Max Magnitude0
ClinVar
Risk rs1057516666(-;-)
Alt rs1057516666(-;-)
Reference Rs1057516666(GT;GT)
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.100346857_100346858delGT
CLNSRC
CLNACC RCV000410044.1,