rs539075, CDH2

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
CUI: C0175697
Disease: Van der Woude syndrome
0.010 GeneticVariation BEFREE Genome-wide linkage analysis and whole genome sequencing in a Van der Woude syndrome (VWS) family revealed that the SNP, rs539075, within intron 2 of the cadherin 2 gene (CDH2) co-segregated with the disease phenotype. 29524576 2018