CCRL2, C-C motif chemokine receptor like 2, 9034

N. diseases: 59; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
A 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C1836233
Disease:
AIDS, PROGRESSION TO
A 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
A 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C0376705
Disease:
Viral Load result
A 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO
A 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C1836233
Disease:
AIDS, PROGRESSION TO
0.700 GeneticVariation GWASCAT Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load. 26553974 2015
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO
0.700 GeneticVariation GWASCAT Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load. 26553974 2015
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 GeneticVariation GWASCAT Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load. 26553974 2015
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 GeneticVariation GWASCAT Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load. 26553974 2015
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C2363741
Disease:
HIV-1 infection
0.700 GeneticVariation GWASCAT Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load. 26553974 2015
dbSNP: rs6808835
rs6808835
Entrez Id: 9034;102724297
Gene Symbol: CCRL2;CCR5AS
CCRL2;CCR5AS
CUI: C0002395
Disease:
Alzheimer's Disease
G 0.700 GeneticVariation GWASCAT Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation. 25340798 2014
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C0019693
Disease:
HIV Infections
0.010 GeneticVariation BEFREE Multiple genome-wide studies have identified associations between outcome of human immunodeficiency virus (HIV) infection and polymorphisms in and around the gene encoding the HIV co-receptor CCR5, but the functional basis for the strongest of these associations, rs1015164A/G, is unknown. 31209403 2019
dbSNP: rs1015164
rs1015164
Entrez Id: 9034
Gene Symbol: CCRL2
CCRL2
CUI: C0021051
Disease:
Immunologic Deficiency Syndromes
0.010 GeneticVariation BEFREE Multiple genome-wide studies have identified associations between outcome of human immunodeficiency virus (HIV) infection and polymorphisms in and around the gene encoding the HIV co-receptor CCR5, but the functional basis for the strongest of these associations, rs1015164A/G, is unknown. 31209403 2019
dbSNP: rs3204849
rs3204849
Entrez Id: 9034;102724297
Gene Symbol: CCRL2;CCR5AS
CCRL2;CCR5AS
CUI: C1535939
Disease:
Pneumocystis jiroveci pneumonia
0.010 GeneticVariation BEFREE Role of exonic variation in chemokine receptor genes on AIDS: CCRL2 F167Y association with pneumocystis pneumonia. 22046140 2011