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rs11525066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs11525066(A;A)
Make rs11525066(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position78546660
GeneMAGI2
is asnp
is mentioned by
dbSNPrs11525066
ebirs11525066
HLIrs11525066
Exacrs11525066
Varsomers11525066
Maprs11525066
PheGenIrs11525066
hapmaprs11525066
1000 genomesrs11525066
hgdprs11525066
ensemblrs11525066
gopubmedrs11525066
geneviewrs11525066
scholarrs11525066
googlers11525066
pharmgkbrs11525066
gwascentralrs11525066
openSNPrs11525066
23andMers11525066
23andMe allrs11525066
SNP Nexus

SNPshotrs11525066
SNPdbers11525066
MSV3drs11525066
GWAS Ctlgrs11525066
GMAF0.04959
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19668339OA-icon.png]
Trait Hippocampal atrophy
Title Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
Risk Allele
P-val 0.000003
Odds Ratio NR NR


GET Evidence
rs11525066
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.046875
summary