Disease: Idiopathic Inflammatory Myopathies ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Idiopathic Inflammatory Myopathies
CUI: C0751356
Disease: Idiopathic Inflammatory Myopathies
0.020 GeneticVariation BEFREE The PTPN22 R620W minor allele is associated with susceptibility to IIM in SA patients, independent of the 8.1 AH. 27312665 2017
Idiopathic Inflammatory Myopathies
CUI: C0751356
Disease: Idiopathic Inflammatory Myopathies
0.020 GeneticVariation BEFREE The R620W variant is a significant risk factor for IIM, independent of the HLA 8.1 haplotype. 18821667 2008