rs1923775
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1923775(C;C) |
| Make rs1923775(C;T) |
| Make rs1923775(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 2101369 |
| Gene | POLN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1923775 |
| dbSNP (classic) | rs1923775 |
| ClinGen | rs1923775 |
| ebi | rs1923775 |
| HLI | rs1923775 |
| Exac | rs1923775 |
| Gnomad | rs1923775 |
| Varsome | rs1923775 |
| LitVar | rs1923775 |
| Map | rs1923775 |
| PheGenI | rs1923775 |
| Biobank | rs1923775 |
| 1000 genomes | rs1923775 |
| hgdp | rs1923775 |
| ensembl | rs1923775 |
| geneview | rs1923775 |
| scholar | rs1923775 |
| rs1923775 | |
| pharmgkb | rs1923775 |
| gwascentral | rs1923775 |
| openSNP | rs1923775 |
| 23andMe | rs1923775 |
| SNPshot | rs1923775 |
| SNPdbe | rs1923775 |
| MSV3d | rs1923775 |
| GWAS Ctlg | rs1923775 |
| GMAF | 0.3962 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22159054 ]
|
| Trait | |
| Title | A comprehensive genetic association study of Alzheimer disease in African Americans. |
| Risk Allele | T |
| P-val | 0.000006 |
| Odds Ratio | 1.6000 None |
