rs2235375, IRF6

N. diseases: 7
Disease: Van der Woude syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Van der Woude syndrome
CUI: C0175697
Disease: Van der Woude syndrome
0.010 GeneticVariation BEFREE To examine the role of the IRF6 mutations in Polish families with Van der Woude syndrome and popliteal pterygium syndrome and to determine the effect of IRF6 single nucleotide polymorphisms (rs7552506, rs2013162, and rs2235375) on cleft lip and/or palate susceptibility. 25489771 2015