rs4509693
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4509693(C;C) |
| Make rs4509693(C;T) |
| Make rs4509693(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 100741814 |
| Gene | PAX2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4509693 |
| dbSNP (classic) | rs4509693 |
| ClinGen | rs4509693 |
| ebi | rs4509693 |
| HLI | rs4509693 |
| Exac | rs4509693 |
| Gnomad | rs4509693 |
| Varsome | rs4509693 |
| LitVar | rs4509693 |
| Map | rs4509693 |
| PheGenI | rs4509693 |
| Biobank | rs4509693 |
| 1000 genomes | rs4509693 |
| hgdp | rs4509693 |
| ensembl | rs4509693 |
| geneview | rs4509693 |
| scholar | rs4509693 |
| rs4509693 | |
| pharmgkb | rs4509693 |
| gwascentral | rs4509693 |
| openSNP | rs4509693 |
| 23andMe | rs4509693 |
| SNPshot | rs4509693 |
| SNPdbe | rs4509693 |
| MSV3d | rs4509693 |
| GWAS Ctlg | rs4509693 |
| GMAF | 0.1708 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19749422] |
| Trait | Alzheimer's Disease |
| Title | Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | NR NR |
| GWAS snp | |
|---|---|
| PMID | [PMID 20061627 |
| Trait | Alzheimer's disease |
| Title | Genome-wide scan of copy number variation in late-onset Alzheimer's disease. |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | None None |
