Diabetes Mellitus, Insulin-Dependent
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.
|
17632545 |
2007 |
Multiple Sclerosis
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Risk alleles for multiple sclerosis identified by a genomewide study.
|
17660530 |
2007 |
Rheumatoid Arthritis
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.
|
17804836 |
2007 |
Psoriasis
|
0.130 |
GeneticVariation
|
disease |
GWASDB |
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci.
|
18369459 |
2008 |
Psoriasis
|
0.130 |
GeneticVariation
|
disease |
GWASCAT |
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci.
|
18369459 |
2008 |
Psoriasis
|
0.130 |
GeneticVariation
|
disease |
BEFREE |
However, rs2395029 encoding the G2V polymorphism within the class I gene HCP5 (combined P = 2.13x10(-26) in U.S. cases) yielded the highest ORs with both PS and PSA (4.1 and 3.2 respectively).
|
18369459 |
2008 |
Salivary Gland Pleomorphic Adenoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
However, rs2395029 encoding the G2V polymorphism within the class I gene HCP5 (combined P = 2.13x10(-26) in U.S. cases) yielded the highest ORs with both PS and PSA (4.1 and 3.2 respectively).
|
18369459 |
2008 |
Human immunodeficiency virus (HIV) II infection category B1
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
This study of 1,103 individuals infected with human immunodeficiency virus assessed the usefulness of genotyping a HCP5 single-nucleotide polymorphism (SNP), rs2395029, in relation to ABC-HSR.
|
18684101 |
2008 |
HIV Infections
|
0.040 |
Biomarker
|
group |
BEFREE |
They specifically demonstrate that the influence of ZNRD1 alleles on disease progression rates are attributable to HLA-A10, help clarify the relationship between the HCP5, HLA-C and HLA-B*57 alleles, and reaffirm a critical role of HLA-B*57 alleles in HIV disease.
|
18982067 |
2008 |
Progressive Neoplastic Disease
|
0.010 |
GeneticVariation
|
phenotype |
BEFREE |
Furthermore, HCP5 and HLA-C alleles stratify B*57-containing genotypes into those that associate with either striking disease retardation or progressive disease, providing one explanation for the long-standing conundrum of why some HLA-B*57-carrying individuals are long-term non-progressors, whereas others exhibit progressive disease.
|
18982067 |
2008 |
Progressive cGVHD
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Furthermore, HCP5 and HLA-C alleles stratify B*57-containing genotypes into those that associate with either striking disease retardation or progressive disease, providing one explanation for the long-standing conundrum of why some HLA-B*57-carrying individuals are long-term non-progressors, whereas others exhibit progressive disease.
|
18982067 |
2008 |
Acute Chest Syndrome
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The minor allele variants of SNPs in the HLA-C and HCP5 gene regions are also in the ACS associated with a lower viral load at set point and additionally with delayed HIV-1 disease progression.
|
19050382 |
2009 |
HIV-1 infection
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Association of HLA-C and HCP5 gene regions with the clinical course of HIV-1 infection.
|
19050382 |
2009 |
Acquired Immunodeficiency Syndrome
|
0.100 |
GeneticVariation
|
group |
GWASDB |
Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).
|
19115949 |
2009 |
Acquired Immunodeficiency Syndrome
|
0.100 |
GeneticVariation
|
group |
GWASCAT |
Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).
|
19115949 |
2009 |
Chemical and Drug Induced Liver Injury
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.
|
19483685 |
2009 |
Chemical and Drug Induced Liver Injury
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.
|
19483685 |
2009 |
Rheumatoid Arthritis
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.
|
19503088 |
2009 |
HIV Infections
|
0.040 |
GeneticVariation
|
group |
BEFREE |
A genome-wide association study of people with incident human immunodeficiency virus (HIV) infection selected from nine different cohorts identified allelic polymorphisms, which associated with either viral set point (HCP5 and 5' HLA-C) or with HIV disease progression (RNF39 and ZNRD1).
|
19693088 |
2009 |
HIV disease progression
|
0.010 |
Biomarker
|
disease |
BEFREE |
The analysis revealed complete linkage disequilibrium between HCP5 and HLA-B*5701/HLA-Cw*06, a modest effect of 5' HLA-C on viral set point in the absence of HLA-B*5701, and no influence of the RNF39 /ZNRD1 extended haplotype on HIV disease progression.
|
19693088 |
2009 |
HIV Infections
|
0.040 |
GeneticVariation
|
group |
BEFREE |
The top two SNPs with the greatest frequency differences between the northern Han and southern Han clusters (F(ST) > 0.06) were found in the FADS2 gene, which associates with the fatty acid composition in phospholipids, and in the HLA complex P5 gene (HCP5), which associates with HIV infection, psoriasis, and psoriatic arthritis.
|
19944404 |
2009 |
Arthritis, Psoriatic
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The top two SNPs with the greatest frequency differences between the northern Han and southern Han clusters (F(ST) > 0.06) were found in the FADS2 gene, which associates with the fatty acid composition in phospholipids, and in the HLA complex P5 gene (HCP5), which associates with HIV infection, psoriasis, and psoriatic arthritis.
|
19944404 |
2009 |
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Common genetic variation and the control of HIV-1 in humans.
|
20041166 |
2009 |
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Common genetic variation and the control of HIV-1 in humans.
|
20041166 |
2009 |
HIV-1, RESISTANCE TO
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Common genetic variation and the control of HIV-1 in humans.
|
20041166 |
2009 |