rs561655
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs561655(A;A) |
Make rs561655(A;G) |
Make rs561655(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 86089237 |
is a | snp |
is | mentioned by |
dbSNP | rs561655 |
dbSNP (classic) | rs561655 |
ClinGen | rs561655 |
ebi | rs561655 |
HLI | rs561655 |
Exac | rs561655 |
Gnomad | rs561655 |
Varsome | rs561655 |
LitVar | rs561655 |
Map | rs561655 |
PheGenI | rs561655 |
Biobank | rs561655 |
1000 genomes | rs561655 |
hgdp | rs561655 |
ensembl | rs561655 |
geneview | rs561655 |
scholar | rs561655 |
rs561655 | |
pharmgkb | rs561655 |
gwascentral | rs561655 |
openSNP | rs561655 |
23andMe | rs561655 |
SNPshot | rs561655 |
SNPdbe | rs561655 |
MSV3d | rs561655 |
GWAS Ctlg | rs561655 |
GMAF | 0.359 |
Max Magnitude | 0 |
? | (A;A) (A;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 19734902] Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.