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rs536906561

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs536906561(A;A)
Make rs536906561(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position80112929
GeneGAA
is asnp
is mentioned by
dbSNPrs536906561
ebirs536906561
HLIrs536906561
Exacrs536906561
Varsomers536906561
Maprs536906561
PheGenIrs536906561
hapmaprs536906561
1000 genomesrs536906561
hgdprs536906561
ensemblrs536906561
gopubmedrs536906561
geneviewrs536906561
scholarrs536906561
googlers536906561
pharmgkbrs536906561
gwascentralrs536906561
openSNPrs536906561
23andMers536906561
23andMe allrs536906561
SNP Nexus

SNPshotrs536906561
SNPdbers536906561
MSV3drs536906561
GWAS Ctlgrs536906561
Max Magnitude0
ClinVar
Risk rs536906561(A;A)
Alt rs536906561(A;A)
Reference rs536906561(G;G)
Significance Probable-Pathogenic
Disease Glycogen storage disease
Variation info
Gene GAA
CLNDBN Glycogen storage disease, type II
Reversed 0
HGVS NC_000017.10:g.78086728G>A
CLNSRC
CLNACC RCV000169262.1,