rs764670582, GJA1

N. diseases: 5
Disease: Syndactyly ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Syndactyly
CUI: C0039075
Disease: Syndactyly
0.010 GeneticVariation BEFREE However, characteristic ocular and dental features of ODDD as well as syndactyly are absent in patients with the recessive Arg239Gln Cx43 mutation. 23951358 2013