rs1373549
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1373549(C;C) |
| Make rs1373549(C;T) |
| Make rs1373549(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 46092055 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1373549 |
| dbSNP (classic) | rs1373549 |
| ClinGen | rs1373549 |
| ebi | rs1373549 |
| HLI | rs1373549 |
| Exac | rs1373549 |
| Gnomad | rs1373549 |
| Varsome | rs1373549 |
| LitVar | rs1373549 |
| Map | rs1373549 |
| PheGenI | rs1373549 |
| Biobank | rs1373549 |
| 1000 genomes | rs1373549 |
| hgdp | rs1373549 |
| ensembl | rs1373549 |
| geneview | rs1373549 |
| scholar | rs1373549 |
| rs1373549 | |
| pharmgkb | rs1373549 |
| gwascentral | rs1373549 |
| openSNP | rs1373549 |
| 23andMe | rs1373549 |
| SNPshot | rs1373549 |
| SNPdbe | rs1373549 |
| MSV3d | rs1373549 |
| GWAS Ctlg | rs1373549 |
| GMAF | 0.3058 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19668339 ]
|
| Trait | Hippocampal atrophy |
| Title | Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease |
| Risk Allele | |
| P-val | 0.000008 |
| Odds Ratio | NR NR |
