rs2280789
| Orientation | minus |
| Stabilized | minus |
| Make rs2280789(C;C) |
| Make rs2280789(C;T) |
| Make rs2280789(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 35879999 |
| Gene | CCL5, LOC105371744 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2280789 |
| dbSNP (classic) | rs2280789 |
| ClinGen | rs2280789 |
| ebi | rs2280789 |
| HLI | rs2280789 |
| Exac | rs2280789 |
| Gnomad | rs2280789 |
| Varsome | rs2280789 |
| LitVar | rs2280789 |
| Map | rs2280789 |
| PheGenI | rs2280789 |
| Biobank | rs2280789 |
| 1000 genomes | rs2280789 |
| hgdp | rs2280789 |
| ensembl | rs2280789 |
| geneview | rs2280789 |
| scholar | rs2280789 |
| rs2280789 | |
| pharmgkb | rs2280789 |
| gwascentral | rs2280789 |
| openSNP | rs2280789 |
| 23andMe | rs2280789 |
| SNPshot | rs2280789 |
| SNPdbe | rs2280789 |
| MSV3d | rs2280789 |
| GWAS Ctlg | rs2280789 |
| GMAF | 0.2034 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21547257
] CCL5/RANTES Gene Polymorphisms in Slavonic Patients with Myocardial Infarction
[PMID 16773571] Genetic variation in the CCL18-CCL3-CCL4 chemokine gene cluster influences HIV Type 1 transmission and AIDS disease progression.
[PMID 17540042] The association of RANTES polymorphism with severe acute respiratory syndrome in Hong Kong and Beijing Chinese.
[PMID 17848170] The chemokine network. II. On how polymorphisms and alternative splicing increase the number of molecular species and configure intricate patterns of disease susceptibility.
[PMID 18217191] Association of CC chemokine ligand 5 genotype with urinary albumin excretion in the non-diabetic Japanese general population: the Takahata study.
[PMID 20041166] Common genetic variation and the control of HIV-1 in humans.
[PMID 20805685] Significant associations between CCL5 gene polymorphisms and post-transplantational diabetes mellitus in Korean renal allograft recipients.
[PMID 23133602] Pharmacogenetics of efficacy and safety of HCV treatment in HCV-HIV coinfected patients: significant associations with IL28B and SOCS3 gene variants.
[PMID 23207898] RANTES polymorphisms and the risk of graft-versus-host disease in human leukocyte antigen-matched sibling allogeneic hematopoietic stem cell transplantation.
