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rs786204467

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204467(A;G)
Make rs786204467(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position80104587
GeneGAA
is asnp
is mentioned by
dbSNPrs786204467
ebirs786204467
HLIrs786204467
Exacrs786204467
Varsomers786204467
Maprs786204467
PheGenIrs786204467
hapmaprs786204467
1000 genomesrs786204467
hgdprs786204467
ensemblrs786204467
gopubmedrs786204467
geneviewrs786204467
scholarrs786204467
googlers786204467
pharmgkbrs786204467
gwascentralrs786204467
openSNPrs786204467
23andMers786204467
23andMe allrs786204467
SNP Nexus

SNPshotrs786204467
SNPdbers786204467
MSV3drs786204467
GWAS Ctlgrs786204467
Max Magnitude0
ClinVar
Risk rs786204467(G;G)
Alt rs786204467(G;G)
Reference rs786204467(A;A)
Significance Probable-Pathogenic
Disease Glycogen storage disease
Variation info
Gene GAA
CLNDBN Glycogen storage disease, type II
Reversed 0
HGVS NC_000017.10:g.78078386A>G
CLNSRC
CLNACC RCV000169114.1,