Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		0.700 Biomarker GENOMICS_ENGLAND Emerging therapeutic targets in the short QT syndrome. 29697308

2018
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		0.700 GeneticVariation UNIPROT KCNQ1 gain-of-function mutation in familial atrial fibrillation. 12522251

2003
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		0.700 Biomarker GENOMICS_ENGLAND Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. 8528244

1996
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		0.700 Biomarker GENOMICS_ENGLAND

Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 3 		0.700 Biomarker CTD_human