Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3741
Gene Symbol: KCNA5
KCNA5
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		0.300 GermlineCausalMutation ORPHANET Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation. 19343045

2009
Entrez Id: 3741
Gene Symbol: KCNA5
KCNA5
CUI: C1843687
Disease: ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder) 		0.300 GermlineCausalMutation ORPHANET Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation. 16772329

2006