Gene: SCN10A ×
Source: CURATED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A 		0.300 Biomarker disease CLINGEN Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population. 27272739 2017
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A 		0.300 Biomarker disease CLINGEN Novel SCN10A variants associated with Brugada syndrome. 25842276 2016
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A 		0.300 Biomarker disease CLINGEN Contrasting Nav1.8 Activity in Scn10a-/- Ventricular Myocytes and the Intact Heart. 27806966 2016
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A 		0.300 Biomarker disease CLINGEN Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. 25691538 2015
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A 		0.300 Biomarker disease CLINGEN Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome. 24998131 2014
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A 		0.300 Biomarker disease CLINGEN A common genetic variant within SCN10A modulates cardiac SCN5A expression. 24642470 2014
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A 		0.300 Biomarker disease CLINGEN Blocking Scn10a channels in heart reduces late sodium current and is antiarrhythmic. 22723299 2012
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A 		0.300 Biomarker disease CLINGEN A tetrodotoxin-resistant voltage-gated sodium channel from human dorsal root ganglia, hPN3/SCN10A. 9839820 1998