Gene: SCN9A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6335
Gene Symbol: SCN9A
SCN9A 		0.020 GeneticVariation group BEFREE Erythromelalgia due to heterozygous gain-of-function SCN9A mutations usually presents as a pure sensory-autonomic disorder characterized by recurrent episodes of burning pain and redness of the extremities. 23893323 2014
Entrez Id: 6335
Gene Symbol: SCN9A
SCN9A 		0.020 Biomarker group BEFREE Autonomic dysfunction in SCN9A-associated primary erythromelalgia. 23152140 2013