rs708486
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs708486(C;C) |
| Make rs708486(C;T) |
| Make rs708486(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 52274253 |
| Gene | PTGDR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs708486 |
| dbSNP (classic) | rs708486 |
| ClinGen | rs708486 |
| ebi | rs708486 |
| HLI | rs708486 |
| Exac | rs708486 |
| Gnomad | rs708486 |
| Varsome | rs708486 |
| LitVar | rs708486 |
| Map | rs708486 |
| PheGenI | rs708486 |
| Biobank | rs708486 |
| 1000 genomes | rs708486 |
| hgdp | rs708486 |
| ensembl | rs708486 |
| geneview | rs708486 |
| scholar | rs708486 |
| rs708486 | |
| pharmgkb | rs708486 |
| gwascentral | rs708486 |
| openSNP | rs708486 |
| 23andMe | rs708486 |
| SNPshot | rs708486 |
| SNPdbe | rs708486 |
| MSV3d | rs708486 |
| GWAS Ctlg | rs708486 |
| GMAF | 0.2865 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21239057
] Polymorphisms in integrin genes and lymphoma risk
