Have questions? Visit https://www.reddit.com/r/SNPedia

rs374470794

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374470794(C;G)
Make rs374470794(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position80112625
GeneGAA
is asnp
is mentioned by
dbSNPrs374470794
ebirs374470794
HLIrs374470794
Exacrs374470794
Varsomers374470794
Maprs374470794
PheGenIrs374470794
hapmaprs374470794
1000 genomesrs374470794
hgdprs374470794
ensemblrs374470794
gopubmedrs374470794
geneviewrs374470794
scholarrs374470794
googlers374470794
pharmgkbrs374470794
gwascentralrs374470794
openSNPrs374470794
23andMers374470794
23andMe allrs374470794
SNP Nexus

SNPshotrs374470794
SNPdbers374470794
MSV3drs374470794
GWAS Ctlgrs374470794
Max Magnitude0
ClinVar
Risk rs374470794(G;G)
Alt rs374470794(G;G)
Reference rs374470794(C;C)
Significance Pathogenic
Disease Glycogen storage disease
Variation info
Gene GAA
CLNDBN Glycogen storage disease, type II
Reversed 0
HGVS NC_000017.10:g.78086424C>T
CLNSRC
CLNACC RCV000174449.1,