Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4730775
rs4730775
0.710 GeneticVariation BEFREE We observed significant association with SNP rs4730775 at the wingless-type MMTV integration site family member 2 (WNT2) locus on chromosome 7 (P = 0.0015, OR 0.61), but found no evidence for the other eight loci being involved with PD despite the large effect size seen for some of these variants in DD. 22489561

2012

dbSNP: rs4730775
rs4730775
0.710 GeneticVariation GWASDB Wnt signaling and Dupuytren's disease. 21732829

2011