Gene: SNX10 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 29887
Gene Symbol: SNX10
SNX10 		0.010 GeneticVariation disease BEFREE Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia. 23123320 2013