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rs796051877

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051877(A;A)
Make rs796051877(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position80110055
GeneGAA
is asnp
is mentioned by
dbSNPrs796051877
ebirs796051877
HLIrs796051877
Exacrs796051877
Varsomers796051877
Maprs796051877
PheGenIrs796051877
hapmaprs796051877
1000 genomesrs796051877
hgdprs796051877
ensemblrs796051877
gopubmedrs796051877
geneviewrs796051877
scholarrs796051877
googlers796051877
pharmgkbrs796051877
gwascentralrs796051877
openSNPrs796051877
23andMers796051877
23andMe allrs796051877
SNP Nexus

SNPshotrs796051877
SNPdbers796051877
MSV3drs796051877
GWAS Ctlgrs796051877
Max Magnitude0
ClinVar
Risk rs796051877(A;A)
Alt rs796051877(A;A)
Reference rs796051877(G;G)
Significance Pathogenic
Disease Glycogen storage disease
Variation info
Gene GAA
CLNDBN Glycogen storage disease, type II
Reversed 0
HGVS NC_000017.10:g.78083854G>A
CLNSRC
CLNACC RCV000186551.1,