rs4246905, TNFSF15

N. diseases: 16
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 Significantly lower frequencies of the C allele and the CC genotype and higher frequencies of the TT and CT genotypes of <i>TNFSF15</i>/rs4246905 were observed in BD patients. 29285231 2017