{{Rsnum
|rsid=1799987
|Gene=CCR5
|Chromosome=3
|position=46370444
|Orientation=plus
|GMAF=0.4871
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CCR5,LOC102724297
}}[[CCR5]] 59029G, also known as -2459 [PMID 9742978, PMID 12815099]

{{PMID Auto
|PMID=22146622
|Title=Polymorphisms of CCL3L1/CCR5 genes and recurrence of hepatitis B in liver transplant recipients
}}

{{PMID Auto
|PMID=15726497
|Title=Gene-environment interaction effects on the development of immune responses in the 1st year of life.
|OA=1
}}

{{PMID Auto
|PMID=17079285
|Title=Genetic protection against hepatitis B virus conferred by CCR5Delta32: Evidence that CCR5 contributes to viral persistence.
|OA=1
}}

{{PMID Auto
|PMID=17672867
|Title=Polymorphisms in chemokine receptor genes and susceptibility to Kawasaki disease.
|OA=1
}}

{{PMID Auto
|PMID=17984846
|Title=Single nucleotide polymorphism of CC chemokine ligand 5 promoter gene in recipients may predict the risk of chronic graft-versus-host disease and its severity after allogeneic transplantation.
}}

{{PMID Auto
|PMID=18182569
|Title=Pharmacogenetics of minimal residual disease response in children with B-precursor acute lymphoblastic leukemia: a report from the Children's Oncology Group.
|OA=1
}}

{{PMID Auto
|PMID=18633107
|Title=G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes.
|OA=1
}}

{{PMID Auto
|PMID=19131662
|Title=A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
|OA=1
}}

{{PMID Auto
|PMID=19225544
|Title=Variation in the lymphotoxin-alpha/tumor necrosis factor locus modifies risk of erythema nodosum in sarcoidosis.
|OA=1
}}

{{PMID Auto
|PMID=19263529
|Title=Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.
|OA=1
}}

{{PMID Auto
|PMID=19330901
|Title=Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=19559392
|Title=A candidate gene association study of 77 polymorphisms in migraine.
|OA=1
}}

{{PMID Auto
|PMID=20031567
|Title=An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=20206716
|Title=Genetic variation within the gene encoding the HIV-1 CCR5 coreceptor in two South African populations.
|OA=1
}}

{{PMID Auto
|PMID=20487506
|Title=A whole genome association study of mother-to-child transmission of HIV in Malawi.
|OA=1
}}

{{PMID Auto
|PMID=20552027
|Title=Host and viral genetic correlates of clinical definitions of HIV-1 disease progression.
|OA=1
}}

{{PMID Auto
|PMID=21091093
|Title=Polymorphisms in chemokine and receptor genes and gastric cancer risk and survival in a high risk Polish population.
|OA=1
}}

{{PMID Auto
|PMID=22924548
|Title=CCR5 gene polymorphism is a genetic risk factor for radiographic severity of rheumatoid arthritis.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}