rs864309487, GMNN

N. diseases: 20
Disease: Congenital small ears ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital small ears
CUI: C0152423
Disease: Congenital small ears
0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015