Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B 		0.300 GermlineCausalMutation disease ORPHANET Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477 2009
Entrez Id: 9631
Gene Symbol: NUP155
NUP155 		0.300 GermlineCausalMutation disease ORPHANET Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death. 19070573 2008
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.300 GermlineCausalMutation disease ORPHANET Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation. 18378609 2008
Entrez Id: 4878
Gene Symbol: NPPA
NPPA 		0.300 GermlineCausalMutation disease ORPHANET Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation. 18614783 2008
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A 		0.300 GermlineCausalMutation disease ORPHANET A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation. 18929244 2008
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9 		0.300 GeneticVariation disease ORPHANET KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation. 17245405 2007
Entrez Id: 3741
Gene Symbol: KCNA5
KCNA5 		0.300 GermlineCausalMutation disease ORPHANET Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation. 16772329 2006
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		0.300 GermlineCausalMutation disease ORPHANET A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation. 15922306 2005
Entrez Id: 9992
Gene Symbol: KCNE2
KCNE2 		0.300 GermlineCausalMutation disease ORPHANET Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation. 15368194 2004
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		0.300 GermlineCausalMutation disease ORPHANET KCNQ1 gain-of-function mutation in familial atrial fibrillation. 12522251 2003