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rs9349407

From SNPedia

Orientationplus
Stabilizedplus
Make rs9349407(C;C)
Make rs9349407(C;G)
Make rs9349407(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position47485642
GeneCD2AP
is asnp
is mentioned by
dbSNPrs9349407
ebirs9349407
HLIrs9349407
Exacrs9349407
Varsomers9349407
Maprs9349407
PheGenIrs9349407
hapmaprs9349407
1000 genomesrs9349407
hgdprs9349407
ensemblrs9349407
gopubmedrs9349407
geneviewrs9349407
scholarrs9349407
googlers9349407
pharmgkbrs9349407
gwascentralrs9349407
openSNPrs9349407
23andMers9349407
23andMe allrs9349407
SNP Nexus

SNPshotrs9349407
SNPdbers9349407
MSV3drs9349407
GWAS Ctlgrs9349407
GMAF0.1905
Max Magnitude
? (C;C) (C;G) (G;G) 28
Alzheimer's disease associated, based on large 2011 study 10.1038/ng.801[PMID 21460841OA-icon.png] Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease


[PMID 23836404OA-icon.png] Genetic Susceptibility for Alzheimer Disease Neuritic Plaque Pathology


[PMID 25092125] Analyzing 54,936 Samples Supports the Association Between CD2AP rs9349407 Polymorphism and Alzheimer's Disease Susceptibility


[PMID 26543236] Risk prediction for sporadic Alzheimer's disease using genetic risk score in the Han Chinese population

[PMID 26680604] Polygenic Analysis of Late-Onset Alzheimer's Disease from Mainland China.