rs3826656
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3826656(A;A) |
| Make rs3826656(A;G) |
| Make rs3826656(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 51223357 |
| Gene | CD33 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3826656 |
| dbSNP (classic) | rs3826656 |
| ClinGen | rs3826656 |
| ebi | rs3826656 |
| HLI | rs3826656 |
| Exac | rs3826656 |
| Gnomad | rs3826656 |
| Varsome | rs3826656 |
| LitVar | rs3826656 |
| Map | rs3826656 |
| PheGenI | rs3826656 |
| Biobank | rs3826656 |
| 1000 genomes | rs3826656 |
| hgdp | rs3826656 |
| ensembl | rs3826656 |
| geneview | rs3826656 |
| scholar | rs3826656 |
| rs3826656 | |
| pharmgkb | rs3826656 |
| gwascentral | rs3826656 |
| openSNP | rs3826656 |
| 23andMe | rs3826656 |
| SNPshot | rs3826656 |
| SNPdbe | rs3826656 |
| MSV3d | rs3826656 |
| GWAS Ctlg | rs3826656 |
| GMAF | 0.3361 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
genomeweb rs4420638 rs11159647 and rs3826656 were also significantly associated with Alzheimer's disease
| GWAS snp | |
|---|---|
| PMID | [PMID 18976728 ]
|
| Trait | Alzheimer's disease |
| Title | Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | NR NR |
[PMID 20574532] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.
[PMID 22167654] Association studies of 19 candidate SNPs with sporadic Alzheimer's disease in the North Chinese Han population.
[PMID 26455864] Association of CD33 and MS4A cluster variants with Alzheimer's disease in East Asian Populations
