Gene: C19orf12 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 83636
Gene Symbol: C19orf12
C19orf12 		0.010 GeneticVariation disease BEFREE A C19orf12 gene mutation should be considered in young children with clinical signs of progressive upper and lower motor neuron disease. 27671242 2016