Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
0.030 GeneticVariation BEFREE p.E148Q variants have no impact on clinical symptoms and laboratory findings in Henoch-Schönlein purpura patients. 30826945 2019
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
0.030 GeneticVariation BEFREE Subjects with rs3743930-GC or CC and rs28940580-GA or AA genotype have the highest HSP risk, compared to subjects with rs3743930-GG and rs28940580-GG genotype; OR (95% CI) was 2.13 (1.52-2.89). 27796522 2017
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
0.030 GeneticVariation BEFREE Our results suggest that MEFV E148Q could be a contributory genetic factor to HSP and HSP-related joint syndromes. 20602240 2010