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rs764622267

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs764622267(C;T)
Make rs764622267(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position80107718
GeneGAA
is asnp
is mentioned by
dbSNPrs764622267
ebirs764622267
HLIrs764622267
Exacrs764622267
Varsomers764622267
Maprs764622267
PheGenIrs764622267
hapmaprs764622267
1000 genomesrs764622267
hgdprs764622267
ensemblrs764622267
gopubmedrs764622267
geneviewrs764622267
scholarrs764622267
googlers764622267
pharmgkbrs764622267
gwascentralrs764622267
openSNPrs764622267
23andMers764622267
23andMe allrs764622267
SNP Nexus

SNPshotrs764622267
SNPdbers764622267
MSV3drs764622267
GWAS Ctlgrs764622267
Max Magnitude0
ClinVar
Risk rs764622267(T;T)
Alt rs764622267(T;T)
Reference rs764622267(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene GAA
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000017.10:g.78081517C>G
CLNSRC
CLNACC RCV000210587.1,