rs6457617, None

N. diseases: 11
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
0.820 GeneticVariation BEFREE The difference in distribution of rs6457617 polymorphism between RA and control cases was comparable [OR = 0.525, p = .079]. 29168332 2018
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
0.820 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761 2011
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
0.820 GeneticVariation BEFREE None of the SNPs tested was associated with RA susceptibility, except rs7021206 in TRAF1 intron 3 (P = 0.0032) and, among the SNPs previously reported, rs6457617 in HLA (P = 4.6 x 10(-35)). 19714643 2009
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
0.820 GeneticVariation GWASCAT Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility. 18668548 2008
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
0.820 GeneticVariation GWASDB Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility. 18668548 2008
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
0.820 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300 2007
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
0.820 GeneticVariation GWASDB Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300 2007
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
0.820 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836 2007
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.800 GeneticVariation GWASCAT Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study. 31050781 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.800 GeneticVariation GWASCAT Genetic variants are major determinants of CSF antibody levels in multiple sclerosis. 25616667 2015
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.800 GeneticVariation GWASCAT Genetic variants are major determinants of CSF antibody levels in multiple sclerosis. 25616667 2015
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
0.800 GeneticVariation GWASDB Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. 21750679 2011
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
0.800 GeneticVariation GWASCAT Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. 21750679 2011
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.800 GeneticVariation GWASCAT A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.800 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
0.800 GeneticVariation GWASDB Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. 20383147 2010
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
0.800 GeneticVariation GWASCAT Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. 20383147 2010
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.800 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530 2007
Thyrotoxic periodic paralysis
CUI: C0268446
Disease: Thyrotoxic periodic paralysis
0.700 GeneticVariation GWASCAT Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study. 31050781 2019
immunoglobulin G index
CUI: C1318233
Disease: immunoglobulin G index
0.700 GeneticVariation GWASCAT Genetic variants are major determinants of CSF antibody levels in multiple sclerosis. 25616667 2015
IgG Index (procedure)
CUI: C1446147
Disease: IgG Index (procedure)
0.700 GeneticVariation GWASCAT Genetic variants are major determinants of CSF antibody levels in multiple sclerosis. 25616667 2015
IgG Index (procedure)
CUI: C1446147
Disease: IgG Index (procedure)
0.700 GeneticVariation GWASCAT Genetic variants are major determinants of CSF antibody levels in multiple sclerosis. 25616667 2015
immunoglobulin G index
CUI: C1318233
Disease: immunoglobulin G index
0.700 GeneticVariation GWASCAT Genetic variants are major determinants of CSF antibody levels in multiple sclerosis. 25616667 2015
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368 2013
Narcolepsy
CUI: C0027404
Disease: Narcolepsy
0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009