rs1342326, None

N. diseases: 9
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 Patients with BD exhibited a significantly higher prevalence of the T/G genotype of rs1342326</span> polymorphism compared with the control group. 30447310 2019