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rs794727051

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794727051(-;-)
Make rs794727051(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position99877702
GeneAGL
is asnp
is mentioned by
dbSNPrs794727051
ebirs794727051
HLIrs794727051
Exacrs794727051
Varsomers794727051
Maprs794727051
PheGenIrs794727051
hapmaprs794727051
1000 genomesrs794727051
hgdprs794727051
ensemblrs794727051
gopubmedrs794727051
geneviewrs794727051
scholarrs794727051
googlers794727051
pharmgkbrs794727051
gwascentralrs794727051
openSNPrs794727051
23andMers794727051
23andMe allrs794727051
SNP Nexus

SNPshotrs794727051
SNPdbers794727051
MSV3drs794727051
GWAS Ctlgrs794727051
Max Magnitude0
ClinVar
Risk rs794727051(;)
Alt rs794727051(;)
Reference rs794727051(T;T)
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.100343258delT
CLNSRC
CLNACC RCV000174259.1,