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rs767882689

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs767882689(-;-)
Make rs767882689(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position80105111
GeneGAA
is asnp
is mentioned by
dbSNPrs767882689
ebirs767882689
HLIrs767882689
Exacrs767882689
Varsomers767882689
Maprs767882689
PheGenIrs767882689
hapmaprs767882689
1000 genomesrs767882689
hgdprs767882689
ensemblrs767882689
gopubmedrs767882689
geneviewrs767882689
scholarrs767882689
googlers767882689
pharmgkbrs767882689
gwascentralrs767882689
openSNPrs767882689
23andMers767882689
23andMe allrs767882689
SNP Nexus

SNPshotrs767882689
SNPdbers767882689
MSV3drs767882689
GWAS Ctlgrs767882689
Max Magnitude0
ClinVar
Risk rs767882689(;)
Alt rs767882689(;)
Reference rs767882689(TG;TG)
Significance Probable-Pathogenic
Disease Glycogen storage disease
Variation info
Gene GAA
CLNDBN Glycogen storage disease, type II
Reversed 0
HGVS NC_000017.10:g.78078910_78078911delTG
CLNSRC
CLNACC RCV000169454.1,