rs689466, PACERR;PTGS2

N. diseases: 33
Disease: Congenital contractural arachnodactyly ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital contractural arachnodactyly
CUI: C0220668
Disease: Congenital contractural arachnodactyly
0.010 GeneticVariation BEFREE Initial analysis identified significant associations between SNP rs2143417 and rs689466 in cyclooxygenase 2 (COX-2) and CCA risk, after adjusting for multiple comparisons (cutoff of P = 0.0028). 26276523 2015