Disease: Brugada Syndrome 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.500 Biomarker disease CLINGEN Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population. 27272739 2017
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.500 Biomarker disease CLINGEN Contrasting Nav1.8 Activity in Scn10a-/- Ventricular Myocytes and the Intact Heart. 27806966 2016
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.500 Biomarker disease CLINGEN Novel SCN10A variants associated with Brugada syndrome. 25842276 2016
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.500 Biomarker disease CLINGEN Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. 25691538 2015
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.500 Biomarker disease CLINGEN Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome. 24998131 2014
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.500 Biomarker disease CLINGEN A common genetic variant within SCN10A modulates cardiac SCN5A expression. 24642470 2014
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.500 Biomarker disease CTD_human Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. 23872634 2013
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.500 Biomarker disease CLINGEN Blocking Scn10a channels in heart reduces late sodium current and is antiarrhythmic. 22723299 2012
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.500 Biomarker disease CLINGEN A tetrodotoxin-resistant voltage-gated sodium channel from human dorsal root ganglia, hPN3/SCN10A. 9839820 1998