rs4149584, TNFRSF1A

N. diseases: 24
Disease: Behcet Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
0.010 GeneticVariation BEFREE The R92Q mutation in patients with Behçet's disease is associated with an increased risk of extracranial venous thrombosis. 15692984 2005