rs7028891, DELEC1

N. diseases: 2
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 A decreased frequency of the A allele of <i>TNFSF8</i>/rs7028891 was observed in BD patients. 29285231 2017