Gene: NKX2-5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.300 GermlineCausalMutation disease ORPHANET A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation. 23525379 2013
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5 		0.300 GermlineCausalMutation disease ORPHANET Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation. 22818067 2012