Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		0.300 GermlineCausalMutation ORPHANET A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation. 24582607

2014
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		0.300 GermlineCausalMutation ORPHANET Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation. 18378609

2008
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		0.300 GermlineCausalMutation ORPHANET A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation. 18929244

2008