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rs1057516471

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516471(-;T)
Make rs1057516471(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position99870407
GeneAGL
is asnp
is mentioned by
dbSNPrs1057516471
dbSNP (old)rs1057516471
ClinGenrs1057516471
ebirs1057516471
HLIrs1057516471
Exacrs1057516471
Gnomadrs1057516471
Varsomers1057516471
Maprs1057516471
PheGenIrs1057516471
Biobankrs1057516471
1000 genomesrs1057516471
hgdprs1057516471
ensemblrs1057516471
gopubmedrs1057516471
geneviewrs1057516471
scholarrs1057516471
googlers1057516471
pharmgkbrs1057516471
gwascentralrs1057516471
openSNPrs1057516471
23andMers1057516471
23andMe allrs1057516471
SNPshotrs1057516471
SNPdbers1057516471
MSV3drs1057516471
GWAS Ctlgrs1057516471
Max Magnitude0
ClinVar
Risk rs1057516471(T;T)
Alt rs1057516471(T;T)
Reference Rs1057516471(-;-)
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.100335963dupT
CLNSRC
CLNACC RCV000412273.1,