rs326946
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs326946(G;G) |
| Make rs326946(G;T) |
| Make rs326946(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 110628530 |
| Gene | ARHGAP20 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs326946 |
| dbSNP (classic) | rs326946 |
| ClinGen | rs326946 |
| ebi | rs326946 |
| HLI | rs326946 |
| Exac | rs326946 |
| Gnomad | rs326946 |
| Varsome | rs326946 |
| LitVar | rs326946 |
| Map | rs326946 |
| PheGenI | rs326946 |
| Biobank | rs326946 |
| 1000 genomes | rs326946 |
| hgdp | rs326946 |
| ensembl | rs326946 |
| geneview | rs326946 |
| scholar | rs326946 |
| rs326946 | |
| pharmgkb | rs326946 |
| gwascentral | rs326946 |
| openSNP | rs326946 |
| 23andMe | rs326946 |
| SNPshot | rs326946 |
| SNPdbe | rs326946 |
| MSV3d | rs326946 |
| GWAS Ctlg | rs326946 |
| GMAF | 0.2778 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 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 | 7E-7 |
| Odds Ratio | .16 unit decrease |
[PMID 15660291] Population structure, admixture, and aging-related phenotypes in African American adults: the Cardiovascular Health Study.
