ARHGAP6, Rho GTPase activating protein 6, 395

N. diseases: 17; N. variants: 20
Disease: Amelogenesis Imperfecta ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		0.010 GeneticVariation disease BEFREE Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6. 23251683 2012