rs9349407
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9349407(C;C) |
Make rs9349407(C;G) |
Make rs9349407(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 47485642 |
Gene | CD2AP |
is a | snp |
is | mentioned by |
dbSNP | rs9349407 |
dbSNP (classic) | rs9349407 |
ClinGen | rs9349407 |
ebi | rs9349407 |
HLI | rs9349407 |
Exac | rs9349407 |
Gnomad | rs9349407 |
Varsome | rs9349407 |
LitVar | rs9349407 |
Map | rs9349407 |
PheGenI | rs9349407 |
Biobank | rs9349407 |
1000 genomes | rs9349407 |
hgdp | rs9349407 |
ensembl | rs9349407 |
geneview | rs9349407 |
scholar | rs9349407 |
rs9349407 | |
pharmgkb | rs9349407 |
gwascentral | rs9349407 |
openSNP | rs9349407 |
23andMe | rs9349407 |
SNPshot | rs9349407 |
SNPdbe | rs9349407 |
MSV3d | rs9349407 |
GWAS Ctlg | rs9349407 |
GMAF | 0.1905 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
Alzheimer's disease associated, based on large 2011 study 10.1038/ng.801
[PMID 21460841] Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
[PMID 23836404] 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.