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rs528367092

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs528367092(A;A)
Make rs528367092(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position80105771
GeneGAA
is asnp
is mentioned by
dbSNPrs528367092
ebirs528367092
HLIrs528367092
Exacrs528367092
Varsomers528367092
Maprs528367092
PheGenIrs528367092
hapmaprs528367092
1000 genomesrs528367092
hgdprs528367092
ensemblrs528367092
gopubmedrs528367092
geneviewrs528367092
scholarrs528367092
googlers528367092
pharmgkbrs528367092
gwascentralrs528367092
openSNPrs528367092
23andMers528367092
23andMe allrs528367092
SNP Nexus

SNPshotrs528367092
SNPdbers528367092
MSV3drs528367092
GWAS Ctlgrs528367092
Max Magnitude0
ClinVar
Risk rs528367092(A,T;A,T)
Alt rs528367092(A,T;A,T)
Reference rs528367092(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.78079570G>A
CLNSRC
CLNACC RCV000169143.1,