Gene: HLA-DQA1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3117
Gene Symbol: HLA-DQA1
HLA-DQA1 		0.040 Biomarker disease BEFREE A recent population-based approach study of SSNS identified HLA-DQA1 and Phospholipase C-Gamma 2 (PLCG2) missense coding variants as candidate loci. 30568185 2019
Entrez Id: 3117
Gene Symbol: HLA-DQA1
HLA-DQA1 		0.040 GeneticVariation disease BEFREE The 2 HLA-DQA1 variants were significantly associated with SSNS in African American children (C34Y: P=5.7 × 10<sup>-11</sup>; OR, 3.53; 95% CI, 2.33-5.42; F41S: P=1.2 × 10<sup>-13</sup>; OR, 4.08; 95% CI, 2.70-6.28), but not with SRNS (C34Y: P=0.6; F41S: P=0.2). 29277510 2018
Entrez Id: 3117
Gene Symbol: HLA-DQA1
HLA-DQA1 		0.040 GeneticVariation disease BEFREE A recent study of a well-defined modest cohort of children with SSNS identified variants in HLA-DQA1 as a risk factor for SSNS. 27470160 2017
Entrez Id: 3117
Gene Symbol: HLA-DQA1
HLA-DQA1 		0.040 GeneticVariation disease BEFREE In conclusion, this exome array study identified HLA-DQA1 and PLCG2 missense coding variants as candidate loci for SSNS. 25349203 2015