Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1855
Gene Symbol: DVL1
DVL1 		0.400 CausalMutation disease CLINVAR WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. 29276006 2018
Entrez Id: 1855
Gene Symbol: DVL1
DVL1 		0.400 CausalMutation disease CLINVAR DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. 26924530 2016
Entrez Id: 1855
Gene Symbol: DVL1
DVL1 		0.400 Biomarker disease GENOMICS_ENGLAND Mutations in DVL1 cause an osteosclerotic form of Robinow syndrome. 25817014 2015
Entrez Id: 1855
Gene Symbol: DVL1
DVL1 		0.400 CausalMutation disease CLINVAR DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome. 25817016 2015
Entrez Id: 1855
Gene Symbol: DVL1
DVL1 		0.400 Biomarker disease GENOMICS_ENGLAND DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome. 25817016 2015
Entrez Id: 1855
Gene Symbol: DVL1
DVL1 		0.400 GeneticVariation disease CLINVAR
Entrez Id: 2535
Gene Symbol: FZD2
FZD2 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 2535
Gene Symbol: FZD2
FZD2 		0.100 CausalMutation disease CLINVAR
Entrez Id: 1857
Gene Symbol: DVL3
DVL3 		0.100 GeneticVariation disease CLINVAR