rs6738962
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common genotype |
| Make rs6738962(A;G) |
| Make rs6738962(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 80054047 |
| Gene | CTNNA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6738962 |
| dbSNP (classic) | rs6738962 |
| ClinGen | rs6738962 |
| ebi | rs6738962 |
| HLI | rs6738962 |
| Exac | rs6738962 |
| Gnomad | rs6738962 |
| Varsome | rs6738962 |
| LitVar | rs6738962 |
| Map | rs6738962 |
| PheGenI | rs6738962 |
| Biobank | rs6738962 |
| 1000 genomes | rs6738962 |
| hgdp | rs6738962 |
| ensembl | rs6738962 |
| geneview | rs6738962 |
| scholar | rs6738962 |
| rs6738962 | |
| pharmgkb | rs6738962 |
| gwascentral | rs6738962 |
| openSNP | rs6738962 |
| 23andMe | rs6738962 |
| SNPshot | rs6738962 |
| SNPdbe | rs6738962 |
| MSV3d | rs6738962 |
| GWAS Ctlg | rs6738962 |
| GMAF | 0.07759 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23535033 ]
|
| Trait | Alzheimer's disease (cognitive decline) |
| Title | Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. |
| Risk Allele | |
| P-val | 1E-8 |
| Odds Ratio | .18 unit decrease |
