rs1449263, None

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
0.700 GeneticVariation GWASCAT Trans-ethnic meta-analysis of white blood cell phenotypes. 25096241 2014
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
0.700 GeneticVariation GWASCAT Trans-ethnic meta-analysis of white blood cell phenotypes. 25096241 2014
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
0.700 GeneticVariation GWASCAT Multiple loci are associated with white blood cell phenotypes. 21738480 2011
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
0.700 GeneticVariation GWASDB Multiple loci are associated with white blood cell phenotypes. 21738480 2011
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
0.700 GeneticVariation GWASCAT Multiple loci are associated with white blood cell phenotypes. 21738480 2011
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.010 GeneticVariation BEFREE Carriage of the C allele of the ITGA4 promoter SNP rs1449263 was independently and weakly increased in MS patients from each population compared to respective controls (P = 0.037 in Basque; and P = 0.042 in Nordic cohorts), though these associations were lost upon application of permutation correction. 17689671 2007