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rs770610356

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770610356(C;T)
Make rs770610356(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position80108811
GeneGAA
is asnp
is mentioned by
dbSNPrs770610356
ebirs770610356
HLIrs770610356
Exacrs770610356
Varsomers770610356
Maprs770610356
PheGenIrs770610356
hapmaprs770610356
1000 genomesrs770610356
hgdprs770610356
ensemblrs770610356
gopubmedrs770610356
geneviewrs770610356
scholarrs770610356
googlers770610356
pharmgkbrs770610356
gwascentralrs770610356
openSNPrs770610356
23andMers770610356
23andMe allrs770610356
SNP Nexus

SNPshotrs770610356
SNPdbers770610356
MSV3drs770610356
GWAS Ctlgrs770610356
Max Magnitude0
ClinVar
Risk rs770610356(T;T)
Alt rs770610356(T;T)
Reference rs770610356(C;C)
Significance Probable-Pathogenic
Disease Glycogen storage disease
Variation info
Gene GAA
CLNDBN Glycogen storage disease, type II
Reversed 0
HGVS NC_000017.10:g.78082610C>T
CLNSRC
CLNACC RCV000169488.1,