WNT8A, Wnt family member 8A, 7478

N. diseases: 7; N. variants: 3
Disease: Atrial Fibrillation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.410 GeneticVariation disease GWASCAT Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. 30061737 2018
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.410 Biomarker disease BEFREE Genome-wide association studies (GWAS) have identified common variants in nine genomic regions associated with AF (KCNN3, PRRX1, PITX2, WNT8A, CAV1, C9orf3, SYNE2, HCN4 and ZFHX3 genes); however, the genetic variability of these risk variants does not explain the entire genetic susceptibility to AF. 25391453 2015
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.410 GeneticVariation disease GWASDB Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366 2012
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.410 GeneticVariation disease GWASCAT Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366 2012
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.410 Biomarker disease CTD_human Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366 2012