rs769068305, IRF6

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
VAN DER WOUDE SYNDROME 1
CUI: C4551864
Disease: VAN DER WOUDE SYNDROME 1
0.700 CausalMutation CLINVAR Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. 19282774 2009