Gene: SCN5A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.040 GeneticVariation disease BEFREE Five of 252 (2.0%) IBS patients had six rare SCN5A mutations that were absent in 377 IBS-negative controls. 29167113 2018
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.040 GeneticVariation disease BEFREE In the muscle, mutations in the SCN5A-encoded voltage-gated sodium channel Na<sub>V</sub>1.5 are associated with irritable bowel syndrome. 27514480 2016
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.040 GeneticVariation disease BEFREE However, a greater percentage of individuals with SCN5A mutations had constipation-predominant IBS (31%) than diarrhea-predominant IBS (10%; P < .05). 24613995 2014
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.040 GeneticVariation disease LHGDN Therefore, our aims were to evaluate SCN5A as a candidate gene involved in the pathogenesis of IBS and to determine physiological consequences of identified mutations. 19056759 2009
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.040 Biomarker disease BEFREE Therefore, our aims were to evaluate SCN5A as a candidate gene involved in the pathogenesis of IBS and to determine physiological consequences of identified mutations. 19056759 2009