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rs794729209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729209(A;A)
Make rs794729209(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position99875455
GeneAGL
is asnp
is mentioned by
dbSNPrs794729209
dbSNP (old)rs794729209
ClinGenrs794729209
ebirs794729209
HLIrs794729209
Exacrs794729209
Gnomadrs794729209
Varsomers794729209
Maprs794729209
PheGenIrs794729209
Biobankrs794729209
1000 genomesrs794729209
hgdprs794729209
ensemblrs794729209
gopubmedrs794729209
geneviewrs794729209
scholarrs794729209
googlers794729209
pharmgkbrs794729209
gwascentralrs794729209
openSNPrs794729209
23andMers794729209
23andMe allrs794729209
SNP Nexus

SNPshotrs794729209
SNPdbers794729209
MSV3drs794729209
GWAS Ctlgrs794729209
Max Magnitude0
ClinVar
Risk rs794729209(A;A)
Alt rs794729209(A;A)
Reference Rs794729209(G;G)
Significance Pathogenic
Disease Glycogen storage disease type III
Variation info
Gene AGL
CLNDBN Glycogen storage disease type III
Reversed 0
HGVS NC_000001.10:g.100341011G>A
CLNSRC
CLNACC RCV000184029.1,