Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 91584
Gene Symbol: PLXNA4
PLXNA4
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.130 GeneticVariation GWASDB PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation. 25043464

2014

Entrez Id: 6311
Gene Symbol: ATXN2
ATXN2
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.100 GeneticVariation GWASDB The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study. 25009551

2014

Entrez Id: 60468
Gene Symbol: BACH2
BACH2
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.420 GeneticVariation GWASDB Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. 24999842

2014

Entrez Id: 117289
Gene Symbol: TAGAP
TAGAP
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.160 GeneticVariation GWASDB Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. 24999842

2014

Entrez Id: 84162
Gene Symbol: KIAA1109
KIAA1109
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.140 GeneticVariation GWASDB Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. 24999842

2014

Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.130 GeneticVariation GWASDB Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. 24999842

2014

Entrez Id: 154215
Gene Symbol: NKAIN2
NKAIN2
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.100 GeneticVariation GWASDB Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. 24999842

2014

Entrez Id: 31
Gene Symbol: ACACA
ACACA
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.100 GeneticVariation GWASDB Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. 24999842

2014

Entrez Id: 100131327
Gene Symbol: UQCRC2P1
UQCRC2P1
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.100 GeneticVariation GWASDB Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. 24999842

2014

Entrez Id: 7299
Gene Symbol: TYR
TYR
CUI: C0025202
Disease: melanoma
melanoma
0.500 GeneticVariation GWASDB Identification of a melanoma susceptibility locus and somatic mutation in TET2. 24980573

2014

Entrez Id: 54790
Gene Symbol: TET2
TET2
CUI: C0025202
Disease: melanoma
melanoma
0.150 GeneticVariation GWASDB Identification of a melanoma susceptibility locus and somatic mutation in TET2. 24980573

2014

Entrez Id: 8558
Gene Symbol: CDK10
CDK10
CUI: C0025202
Disease: melanoma
melanoma
0.100 GeneticVariation GWASDB Identification of a melanoma susceptibility locus and somatic mutation in TET2. 24980573

2014

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: 2475
Gene Symbol: MTOR
MTOR
CUI: C0524957
Disease: Corneal Topography
Corneal Topography
0.100 GeneticVariation GWASDB CMPK1 and RBP3 are associated with corneal curvature in Asian populations. 24963161

2014

Entrez Id: 5949
Gene Symbol: RBP3
RBP3
CUI: C0524957
Disease: Corneal Topography
Corneal Topography
0.100 GeneticVariation GWASDB CMPK1 and RBP3 are associated with corneal curvature in Asian populations. 24963161

2014

Entrez Id: 9639
Gene Symbol: ARHGEF10
ARHGEF10
CUI: C0524957
Disease: Corneal Topography
Corneal Topography
0.100 GeneticVariation GWASDB CMPK1 and RBP3 are associated with corneal curvature in Asian populations. 24963161

2014

Entrez Id: 9895
Gene Symbol: TECPR2
TECPR2
CUI: C1853959
Disease: Birdshot chorioretinopathy
Birdshot chorioretinopathy
0.100 GeneticVariation GWASDB A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy. 24957906

2014

Entrez Id: 4012
Gene Symbol: LNPEP
LNPEP
CUI: C1853959
Disease: Birdshot chorioretinopathy
Birdshot chorioretinopathy
0.100 GeneticVariation GWASDB A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy. 24957906

2014

Entrez Id: 56547
Gene Symbol: MMP26
MMP26
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.100 GeneticVariation GWASDB Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. 24954895

2014

Entrez Id: 51241
Gene Symbol: COX16
COX16
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.100 GeneticVariation GWASDB Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. 24954895

2014

Entrez Id: 100528007
Gene Symbol: BORCS7-ASMT
BORCS7-ASMT
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.100 GeneticVariation GWASDB Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. 24954895

2014

Entrez Id: 4883
Gene Symbol: NPR3
NPR3
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.100 GeneticVariation GWASDB Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. 24954895

2014

Entrez Id: 64359
Gene Symbol: NXN
NXN
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.100 GeneticVariation GWASDB Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. 24954895

2014

Entrez Id: 114792
Gene Symbol: KLHL32
KLHL32
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.100 GeneticVariation GWASDB Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. 24954895

2014

Entrez Id: 55333
Gene Symbol: SYNJ2BP
SYNJ2BP
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.100 GeneticVariation GWASDB Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. 24954895

2014