rs10895547
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10895547(C;C) |
| Make rs10895547(C;T) |
| Make rs10895547(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 103937424 |
| Gene | PDGFD |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10895547 |
| dbSNP (classic) | rs10895547 |
| ClinGen | rs10895547 |
| ebi | rs10895547 |
| HLI | rs10895547 |
| Exac | rs10895547 |
| Gnomad | rs10895547 |
| Varsome | rs10895547 |
| LitVar | rs10895547 |
| Map | rs10895547 |
| PheGenI | rs10895547 |
| Biobank | rs10895547 |
| 1000 genomes | rs10895547 |
| hgdp | rs10895547 |
| ensembl | rs10895547 |
| geneview | rs10895547 |
| scholar | rs10895547 |
| rs10895547 | |
| pharmgkb | rs10895547 |
| gwascentral | rs10895547 |
| openSNP | rs10895547 |
| 23andMe | rs10895547 |
| SNPshot | rs10895547 |
| SNPdbe | rs10895547 |
| MSV3d | rs10895547 |
| GWAS Ctlg | rs10895547 |
| GMAF | 0.3347 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21347282 ]
|
| Trait | |
| Title | Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project |
| Risk Allele | T |
| P-val | 0.000003 |
| Odds Ratio | 0.0747 [0.04-0.10] SD decrease |
