Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7021
Gene Symbol: TFAP2B
TFAP2B
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.100 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011
Entrez Id: 105377391
Gene Symbol: LINC02264
LINC02264
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.100 GeneticVariation GWASDB A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis. 24978480

2014
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.700 GeneticVariation GWASDB A combined analysis of genome-wide association studies in breast cancer. 20872241

2011
Entrez Id: 643714
Gene Symbol: CASC16
CASC16
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.200 GeneticVariation GWASDB A combined analysis of genome-wide association studies in breast cancer. 20872241

2011
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.100 GeneticVariation GWASDB A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. 16648850

2006
Entrez Id: 5820
Gene Symbol: PVT1
PVT1
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.120 GeneticVariation GWASDB A common variant at 8q24.21 is associated with renal cell cancer. 24220699

2013
Entrez Id: 84700
Gene Symbol: MYO18B
MYO18B
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.100 GeneticVariation GWASDB A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. 23423138

2013
Entrez Id: 23019
Gene Symbol: CNOT1
CNOT1
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.100 GeneticVariation GWASDB A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval. 22726844

2012
Entrez Id: 6546
Gene Symbol: SLC8A1
SLC8A1
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.100 GeneticVariation GWASDB A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval. 22726844

2012
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.100 GeneticVariation GWASDB A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval. 22726844

2012
Entrez Id: 79068
Gene Symbol: FTO
FTO
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.100 GeneticVariation GWASDB A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. 17434869

2007
Entrez Id: 79068
Gene Symbol: FTO
FTO
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.100 GeneticVariation GWASDB A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. 17434869

2007
Entrez Id: 8091
Gene Symbol: HMGA2
HMGA2
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A common variant of HMGA2 is associated with adult and childhood height in the general population. 17767157

2007
Entrez Id: 26137
Gene Symbol: ZBTB20
ZBTB20
CUI: C0489786
Disease: Height
Height 		0.100 GeneticVariation GWASDB A common variant of HMGA2 is associated with adult and childhood height in the general population. 17767157

2007
Entrez Id: 100048912
Gene Symbol: CDKN2B-AS1
CDKN2B-AS1
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.150 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679

2007
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 GeneticVariation GWASDB A comprehensive family-based replication study of schizophrenia genes. 23894747

2013
Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.500 GeneticVariation GWASDB A comprehensive family-based replication study of schizophrenia genes. 23894747

2013
Entrez Id: 23774
Gene Symbol: BRD1
BRD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.500 GeneticVariation GWASDB A comprehensive family-based replication study of schizophrenia genes. 23894747

2013
Entrez Id: 94026
Gene Symbol: POM121L2
POM121L2
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.100 GeneticVariation GWASDB A comprehensive family-based replication study of schizophrenia genes. 23894747

2013
Entrez Id: 5819
Gene Symbol: NECTIN2
NECTIN2
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.440 GeneticVariation GWASDB A comprehensive genetic association study of Alzheimer disease in African Americans. 22159054

2011
Entrez Id: 2153
Gene Symbol: F5
F5
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		0.200 GeneticVariation GWASDB A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array. 23188048

2013
Entrez Id: 3273
Gene Symbol: HRG
HRG
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance 		0.110 GeneticVariation GWASDB A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array. 23188048

2013
Entrez Id: 3273
Gene Symbol: HRG
HRG
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.100 GeneticVariation GWASDB A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array. 23188048

2013
Entrez Id: 6569
Gene Symbol: SLC34A1
SLC34A1
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.100 GeneticVariation GWASDB A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array. 23188048

2013
Entrez Id: 2161
Gene Symbol: F12
F12
CUI: C0030605
Disease: Activated Partial Thromboplastin Time measurement
Activated Partial Thromboplastin Time measurement 		0.100 GeneticVariation GWASDB A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array. 23188048

2013