Gene: CNTN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2 		0.110 GeneticVariation phenotype BEFREE Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. 23518707 2013
Entrez Id: 6900
Gene Symbol: CNTN2
CNTN2 		0.110 Biomarker phenotype HPO