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

rs786204621

From SNPedia

Orientationplus
Geno Mag Summary
(ACA;ACA) 0 common in clinvar
Make rs786204621(-;-)
Make rs786204621(-;ACA)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position80113011
GeneGAA
is asnp
is mentioned by
dbSNPrs786204621
ebirs786204621
HLIrs786204621
Exacrs786204621
Varsomers786204621
Maprs786204621
PheGenIrs786204621
hapmaprs786204621
1000 genomesrs786204621
hgdprs786204621
ensemblrs786204621
gopubmedrs786204621
geneviewrs786204621
scholarrs786204621
googlers786204621
pharmgkbrs786204621
gwascentralrs786204621
openSNPrs786204621
23andMers786204621
23andMe allrs786204621
SNP Nexus

SNPshotrs786204621
SNPdbers786204621
MSV3drs786204621
GWAS Ctlgrs786204621
Max Magnitude0
ClinVar
Risk rs786204621(;)
Alt rs786204621(;)
Reference rs786204621(ACA;ACA)
Significance Probable-Pathogenic
Disease Glycogen storage disease
Variation info
Gene GAA
CLNDBN Glycogen storage disease, type II
Reversed 0
HGVS NC_000017.10:g.78086810_78086812delACA
CLNSRC
CLNACC RCV000169390.1,