|
Lupus Erythematosus, Systemic
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry.
|
26316170 |
2016 |
|
Lupus Erythematosus, Systemic
|
|
0.800 |
GeneticVariation
|
GWASDB |
GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.
|
24871463 |
2014 |
|
Membranous glomerulonephritis
|
|
0.800 |
GeneticVariation
|
GWASDB |
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.
|
21323541 |
2011 |
|
Membranous glomerulonephritis
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.
|
21323541 |
2011 |
|
Lupus Erythematosus, Systemic
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.
|
21408207 |
2011 |
|
Lupus Erythematosus, Systemic
|
|
0.800 |
GeneticVariation
|
GWASDB |
Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.
|
21408207 |
2011 |
|
Celiac Disease
|
|
0.800 |
GeneticVariation
|
GWASDB |
Multiple common variants for celiac disease influencing immune gene expression.
|
20190752 |
2010 |
|
Celiac Disease
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Multiple common variants for celiac disease influencing immune gene expression.
|
20190752 |
2010 |
|
Lupus Erythematosus, Systemic
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.
|
18204098 |
2008 |
|
Lupus Erythematosus, Systemic
|
|
0.800 |
GeneticVariation
|
GWASDB |
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.
|
18204098 |
2008 |
|
Celiac Disease
|
|
0.800 |
GeneticVariation
|
GWASDB |
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.
|
17558408 |
2007 |
|
Celiac Disease
|
|
0.800 |
GeneticVariation
|
GWASCAT |
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.
|
17558408 |
2007 |
|
Autoimmune Chronic Hepatitis
|
|
0.710 |
GeneticVariation
|
BEFREE |
We associated AIH with a variant in the major histocompatibility complex region at rs2187668 (P = 1.5 × 10(-78)).
|
24768677 |
2014 |
|
Autoimmune Chronic Hepatitis
|
|
0.710 |
GeneticVariation
|
GWASCAT |
Genome-wide association study identifies variants associated with autoimmune hepatitis type 1.
|
24768677 |
2014 |
|
Colitis, Collagenous
|
|
0.700 |
GeneticVariation
|
GWASCAT |
Dense genotyping of immune-related loci identifies HLA variants associated with increased risk of collagenous colitis.
|
26525574 |
2017 |
|
Diastolic blood pressure
|
|
0.700 |
GeneticVariation
|
GWASCAT |
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.
|
27618452 |
2016 |
|
Sarcoidosis
|
|
0.700 |
GeneticVariation
|
GWASCAT |
High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences.
|
26651848 |
2016 |
|
Inflammatory Bowel Diseases
|
|
0.700 |
GeneticVariation
|
GWASCAT |
Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.
|
28008999 |
2016 |
|
Lupus Erythematosus, Cutaneous
|
|
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus.
|
25827949 |
2015 |
|
Autoimmune Hepatitis with Centrilobular Necrosis
|
|
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide association study identifies variants associated with autoimmune hepatitis type 1.
|
24768677 |
2014 |
|
Malignant neoplasm of lung
|
|
0.700 |
GeneticVariation
|
GWASDB |
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
|
22899653 |
2012 |
|
Myasthenia Gravis
|
|
0.700 |
GeneticVariation
|
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
|
Asthma
|
|
0.700 |
GeneticVariation
|
GWASDB |
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.
|
21150878 |
2011 |
|
Rheumatoid Arthritis
|
|
0.700 |
GeneticVariation
|
GWASDB |
A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis.
|
21156761 |
2011 |
|
Immunoglobulin A measurement
|
|
0.700 |
GeneticVariation
|
GWASDB |
Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.
|
20694011 |
2010 |