rs2269067, C5

N. diseases: 5
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 Increased frequencies of the GG genotype of C3 rs408290 and C5 rs2269067 were found in BD. 26269006 2015