Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population. 27272739 2017
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN Novel SCN10A variants associated with Brugada syndrome. 25842276 2016
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN Contrasting Nav1.8 Activity in Scn10a-/- Ventricular Myocytes and the Intact Heart. 27806966 2016
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. 25691538 2015
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome. 24998131 2014
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN A common genetic variant within SCN10A modulates cardiac SCN5A expression. 24642470 2014
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN Blocking Scn10a channels in heart reduces late sodium current and is antiarrhythmic. 22723299 2012
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN A tetrodotoxin-resistant voltage-gated sodium channel from human dorsal root ganglia, hPN3/SCN10A. 9839820 1998