Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 401247
Gene Symbol: LINC00243
LINC00243
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
0.100 GeneticVariation GWASCAT Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease. 31169883

2019

Entrez Id: 4439
Gene Symbol: MSH5
MSH5
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
0.100 GeneticVariation GWASCAT Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease. 31169883

2019

Entrez Id: 101929163
Gene Symbol: TSBP1-AS1
TSBP1-AS1
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
0.100 GeneticVariation GWASCAT Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease. 31169883

2019

Entrez Id: 3106
Gene Symbol: HLA-B
HLA-B
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
0.100 GeneticVariation GWASCAT Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease. 31169883

2019

Entrez Id: 100532732
Gene Symbol: MSH5-SAPCD1
MSH5-SAPCD1
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
0.100 GeneticVariation GWASCAT Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease. 31169883

2019

Entrez Id: 9656
Gene Symbol: MDC1
MDC1
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
0.100 GeneticVariation GWASCAT Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease. 31169883

2019

Entrez Id: 259197
Gene Symbol: NCR3
NCR3
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement
0.100 GeneticVariation GWASCAT Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease. 31169883

2019

Entrez Id: 288
Gene Symbol: ANK3
ANK3
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.120 GeneticVariation GWASCAT Genome-wide association study of behavioural and psychiatric features in human prion disease. 25897833

2015

Entrez Id: 5959
Gene Symbol: RDH5
RDH5
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 100506035
Gene Symbol: LINC00989
LINC00989
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 4642
Gene Symbol: MYO1D
MYO1D
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 729911
Gene Symbol: ANKRD34C-AS1
ANKRD34C-AS1
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. 20835236

2010

Entrez Id: 5923
Gene Symbol: RASGRF1
RASGRF1
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 5095
Gene Symbol: PCCA
PCCA
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 9414
Gene Symbol: TJP2
TJP2
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 55349
Gene Symbol: CHDH
CHDH
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. 23474815

2013

Entrez Id: 776
Gene Symbol: CACNA1D
CACNA1D
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 6096
Gene Symbol: RORB
RORB
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 79698
Gene Symbol: ZMAT4
ZMAT4
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 1146
Gene Symbol: CHRNG
CHRNG
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 54715
Gene Symbol: RBFOX1
RBFOX1
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 5801
Gene Symbol: PTPRR
PTPRR
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013

Entrez Id: 55748
Gene Symbol: CNDP2
CNDP2
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
0.100 GeneticVariation GWASCAT Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. 23396134

2013