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rs794729208

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729208(A;A)
Make rs794729208(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position99864536
GeneAGL
is asnp
is mentioned by
dbSNPrs794729208
ebirs794729208
HLIrs794729208
Exacrs794729208
Varsomers794729208
Maprs794729208
PheGenIrs794729208
hapmaprs794729208
1000 genomesrs794729208
hgdprs794729208
ensemblrs794729208
gopubmedrs794729208
geneviewrs794729208
scholarrs794729208
googlers794729208
pharmgkbrs794729208
gwascentralrs794729208
openSNPrs794729208
23andMers794729208
23andMe allrs794729208
SNP Nexus

SNPshotrs794729208
SNPdbers794729208
MSV3drs794729208
GWAS Ctlgrs794729208
Max Magnitude0
ClinVar
Risk rs794729208(A;A)
Alt rs794729208(A;A)
Reference rs794729208(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.100330092T>A
CLNSRC
CLNACC RCV000184029.1,