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rs786204661

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204661(-;-)
Make rs786204661(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position80104951
GeneGAA
is asnp
is mentioned by
dbSNPrs786204661
ebirs786204661
HLIrs786204661
Exacrs786204661
Varsomers786204661
Maprs786204661
PheGenIrs786204661
hapmaprs786204661
1000 genomesrs786204661
hgdprs786204661
ensemblrs786204661
gopubmedrs786204661
geneviewrs786204661
scholarrs786204661
googlers786204661
pharmgkbrs786204661
gwascentralrs786204661
openSNPrs786204661
23andMers786204661
23andMe allrs786204661
SNP Nexus

SNPshotrs786204661
SNPdbers786204661
MSV3drs786204661
GWAS Ctlgrs786204661
Max Magnitude0
ClinVar
Risk rs786204661(;)
Alt rs786204661(;)
Reference rs786204661(T;T)
Significance Probable-Pathogenic
Disease Glycogen storage disease
Variation info
Gene GAA
CLNDBN Glycogen storage disease, type II
Reversed 0
HGVS NC_000017.10:g.78078750delT
CLNSRC
CLNACC RCV000169456.1,