Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4624
Gene Symbol: MYH6
MYH6
0.600 Biomarker disease HPO
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5
0.430 Biomarker disease HPO
Entrez Id: 2626
Gene Symbol: GATA4
GATA4
0.410 GeneticVariation disease CLINVAR
Entrez Id: 2627
Gene Symbol: GATA6
GATA6
0.400 Biomarker disease HPO
Entrez Id: 4763
Gene Symbol: NF1
NF1
0.100 Biomarker disease HPO
Entrez Id: 6135
Gene Symbol: RPL11
RPL11
0.100 Biomarker disease HPO
Entrez Id: 2657
Gene Symbol: GDF1
GDF1
0.100 Biomarker disease HPO
Entrez Id: 23118
Gene Symbol: TAB2
TAB2
0.100 GeneticVariation disease CLINVAR
Entrez Id: 2153
Gene Symbol: F5
F5
0.040 Biomarker disease BEFREE Factor V Leiden and prothrombin gene mutation may predispose to paradoxical embolism in subjects with patent foramen ovale. 12695749 2003
Entrez Id: 100128998
Gene Symbol: C20orf181
C20orf181
0.010 Biomarker disease BEFREE Tissue Plasminogen Activator to Treat a Stroke after Foam Sclerotherapy in a Woman with a Patent Foramen Ovale. 29402614 2018
Entrez Id: 23530
Gene Symbol: NNT
NNT
0.010 Biomarker disease BEFREE NNT for stroke was 37 and NNH for AF 49, indicating a net clinical benefit of PFO closure. 29644412 2018
Entrez Id: 57057
Gene Symbol: TBX20
TBX20
0.300 GermlineCausalMutation disease ORPHANET A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects. 19762328 2010
Entrez Id: 2627
Gene Symbol: GATA6
GATA6
0.400 GermlineCausalMutation disease ORPHANET A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect. 20631719 2010
Entrez Id: 2626
Gene Symbol: GATA4
GATA4
0.410 GermlineCausalMutation disease ORPHANET A novel mutation in GATA4 gene associated with dominant inherited familial atrial septal defect. 20347099 2010
Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11
0.110 CausalMutation disease CLINVAR A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. 29555671 2018
Entrez Id: 6910
Gene Symbol: TBX5
TBX5
0.100 CausalMutation disease CLINVAR A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. 29555671 2018
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5
0.430 GermlineCausalMutation disease ORPHANET Ablation of Nkx2-5 at mid-embryonic stage results in premature lethality and cardiac malformation. 21285290 2011
Entrez Id: 2147
Gene Symbol: F2
F2
0.040 GeneticVariation disease BEFREE Across the population the presence of the FII G20210A mutation (OR: 2.97;95% CI: 1.32-6.69), a history of DVT (OR: 1.04; 95% CI: 1.02-1.06), and oestrogen-containing contraceptive therapy (OR: 1.14; 95% CI: 1.09-1.18) were all associated with stroke of unknown cause after adjustment for other risk factors, This was not the case with PFO. 22909823 2012
Entrez Id: 2153
Gene Symbol: F5
F5
0.040 GeneticVariation disease BEFREE After adjustment for other vascular risk factors, the combination of either factor V Leiden or prothrombin G20210A and PFO was associated with a 4.7-fold (95% CI=1.4 to 16.1; P=0.008) increased risk of cerebral ischemia in young patients. 17525392 2007
Entrez Id: 2147
Gene Symbol: F2
F2
0.040 GeneticVariation disease BEFREE After adjustment for other vascular risk factors, the combination of either factor V Leiden or prothrombin G20210A and PFO was associated with a 4.7-fold (95% CI=1.4 to 16.1; P=0.008) increased risk of cerebral ischemia in young patients. 17525392 2007
Entrez Id: 64805
Gene Symbol: P2RY12
P2RY12
0.020 Biomarker disease BEFREE After finding that the thienopyridines clopidogrel and prasugrel reduced migraine headache (MHA) symptoms in some patients with patent foramen ovale (PFO), this small pilot study was undertaken to determine whether ticagrelor, a nonthienopyridine P2Y12 inhibitor, would have similar MHA effects and might be better suited for a future randomized trial. 30478067 2018
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5
0.430 GeneticVariation disease BEFREE Aim of the present study was to screen a Moroccan population with ASDII for NKX2-5 variants and to assess risk factors that may contribute to emergence of the disorder. 27752029 2017
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.310 GermlineCausalMutation disease ORPHANET Alpha-cardiac actin mutations produce atrial septal defects. 17947298 2008
Entrez Id: 4488
Gene Symbol: MSX2
MSX2
0.010 GeneticVariation disease BEFREE Between January 2012 and August 2016, 151 patients (mean age 41 ± 11 years) who had suffered from a cryptogenic thromboembolic event underwent transcatheter PFO closure with the PFM Nit-Occlud PFO device. 29068141 2018
Entrez Id: 414
Gene Symbol: ARSD
ARSD
0.030 Biomarker disease BEFREE Conscious sedation for transcatheter implantation of ASO is a feasible, safe, and efficient technique, allowing successful PFO and ASD closure in the majority of patients. 29131286 2018