Gene: ZFHX3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 GeneticVariation disease GWASDB Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366 2012
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 GeneticVariation disease GWASCAT Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366 2012
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 Biomarker disease CTD_human Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366 2012
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 Biomarker disease BEFREE Recent genome-wide association studies have identified 3 loci, on chromosomes 4q25 (near PITX2), 16q22 (in ZFHX3), and 1q21 (in KCNN3), that associate with either typical or lone AF. 22726630 2012
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 GeneticVariation disease BEFREE Each of these underlying pathologies may have a specific genetic architecture.Previous genome-wide association studies (GWAS) showed association of variants near PITX2 and ZFHX3 with atrial fibrillation and stroke. 22776031 2012
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 Biomarker disease BEFREE The study expands the association between ZFHX3 and AF to a non-European ancestry population and provides the first evidence of a cross-race susceptibility of the 16q22 AF locus. 21107608 2011
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 GeneticVariation disease GWASCAT Meta-analyses of 896 prevalent (15,768 referents) and 2,517 incident (21,337 referents) AF cases identified a new locus for AF (ZFHX3, rs2106261, risk ratio RR = 1.19; P = 2.3 x 10(-7)). 19597492 2009
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 GeneticVariation disease BEFREE Meta-analyses of 896 prevalent (15,768 referents) and 2,517 incident (21,337 referents) AF cases identified a new locus for AF (ZFHX3, rs2106261, risk ratio RR = 1.19; P = 2.3 x 10(-7)). 19597492 2009
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 GeneticVariation disease BEFREE A variant in the ZFHX3 gene on chromosome 16q22, rs7193343-T, associated significantly with AF (odds ratio OR = 1.21, P = 1.4 x 10(-10)). 19597491 2009
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 GeneticVariation disease GWASDB A variant in the ZFHX3 gene on chromosome 16q22, rs7193343-T, associated significantly with AF (odds ratio OR = 1.21, P = 1.4 x 10(-10)). 19597491 2009
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 GeneticVariation disease GWASCAT A variant in the ZFHX3 gene on chromosome 16q22, rs7193343-T, associated significantly with AF (odds ratio OR = 1.21, P = 1.4 x 10(-10)). 19597491 2009
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 Biomarker disease CTD_human A variant in the ZFHX3 gene on chromosome 16q22, rs7193343-T, associated significantly with AF (odds ratio OR = 1.21, P = 1.4 x 10(-10)). 19597491 2009
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 Biomarker disease CTD_human Meta-analyses of 896 prevalent (15,768 referents) and 2,517 incident (21,337 referents) AF cases identified a new locus for AF (ZFHX3, rs2106261, risk ratio RR = 1.19; P = 2.3 x 10(-7)). 19597492 2009
Entrez Id: 463
Gene Symbol: ZFHX3
ZFHX3 		0.500 GeneticVariation disease GWASDB Meta-analyses of 896 prevalent (15,768 referents) and 2,517 incident (21,337 referents) AF cases identified a new locus for AF (ZFHX3, rs2106261, risk ratio RR = 1.19; P = 2.3 x 10(-7)). 19597492 2009