Source: GWASCAT

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 8638
Gene Symbol: OASL
OASL 		2'-5'-oligoadenylate synthetase like 0.729 0.385 2.8E-11
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		disease 0.100 None 1.000 2 2 2010 2017
Entrez Id: 8638
Gene Symbol: OASL
OASL 		2'-5'-oligoadenylate synthetase like 0.729 0.385 2.8E-11
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		phenotype 0.100 None 1.000 1 1 2013 2018
Entrez Id: 8638
Gene Symbol: OASL
OASL 		2'-5'-oligoadenylate synthetase like 0.729 0.385 2.8E-11
CUI: C0596887
Disease: mathematical ability
mathematical ability 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 8638
Gene Symbol: OASL
OASL 		2'-5'-oligoadenylate synthetase like 0.729 0.385 2.8E-11
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		phenotype 0.100 None 1.000 1 1 2011 2011
Entrez Id: 84890
Gene Symbol: ADO
ADO 		2-aminoethanethiol dioxygenase 0.670 0.538 0.48
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		phenotype 0.100 None 1.000 2 1 2016 2016
Entrez Id: 84890
Gene Symbol: ADO
ADO 		2-aminoethanethiol dioxygenase 0.670 0.538 0.48
CUI: C0001925
Disease: Albuminuria
Albuminuria 		phenotype 0.100 None 1.000 1 2 2018 2018
Entrez Id: 84890
Gene Symbol: ADO
ADO 		2-aminoethanethiol dioxygenase 0.670 0.538 0.48
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		group 0.100 None 1.000 1 1 2019 2019
Entrez Id: 84890
Gene Symbol: ADO
ADO 		2-aminoethanethiol dioxygenase 0.670 0.538 0.48
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 92370
Gene Symbol: PXYLP1
PXYLP1 		2-phosphoxylose phosphatase 1 1.000 0.038 3.1E-03
CUI: C0005890
Disease: Body Height
Body Height 		phenotype 0.100 None 1.000 2 4 2017 2019
Entrez Id: 92370
Gene Symbol: PXYLP1
PXYLP1 		2-phosphoxylose phosphatase 1 1.000 0.038 3.1E-03
CUI: C0005910
Disease: Body Weight
Body Weight 		phenotype 0.100 None 1.000 1 1 2017 2017
Entrez Id: 92370
Gene Symbol: PXYLP1
PXYLP1 		2-phosphoxylose phosphatase 1 1.000 0.038 3.1E-03
CUI: C0027092
Disease: Myopia
Myopia 		disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 92370
Gene Symbol: PXYLP1
PXYLP1 		2-phosphoxylose phosphatase 1 1.000 0.038 3.1E-03
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		phenotype 0.100 None 1.000 1 1 2016 2016
Entrez Id: 92370
Gene Symbol: PXYLP1
PXYLP1 		2-phosphoxylose phosphatase 1 1.000 0.038 3.1E-03
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		phenotype 0.100 None 1.000 1 1 2016 2016
Entrez Id: 92370
Gene Symbol: PXYLP1
PXYLP1 		2-phosphoxylose phosphatase 1 1.000 0.038 3.1E-03
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 1718
Gene Symbol: DHCR24
DHCR24 		24-dehydrocholesterol reductase 0.498 0.769 3.1E-02
CUI: C0005890
Disease: Body Height
Body Height 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 3155
Gene Symbol: HMGCL
HMGCL 		3-hydroxy-3-methylglutaryl-CoA lyase 0.691 0.462 2.6E-06
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		phenotype 0.100 None 1.000 1 1 2016 2016
Entrez Id: 3156
Gene Symbol: HMGCR
HMGCR 		3-hydroxy-3-methylglutaryl-CoA reductase 0.529 0.692 1.00
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		phenotype 0.100 None 1.000 17 8 2008 2019
Entrez Id: 3156
Gene Symbol: HMGCR
HMGCR 		3-hydroxy-3-methylglutaryl-CoA reductase 0.529 0.692 1.00
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		phenotype 0.100 None 1.000 10 7 2009 2019
Entrez Id: 3156
Gene Symbol: HMGCR
HMGCR 		3-hydroxy-3-methylglutaryl-CoA reductase 0.529 0.692 1.00
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		group 0.200 None 1.000 1 1 2008 2020
Entrez Id: 3158
Gene Symbol: HMGCS2
HMGCS2 		3-hydroxy-3-methylglutaryl-CoA synthase 2 0.666 0.577 4.3E-14
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		group 0.100 None 1.000 1 1 2018 2018
Entrez Id: 3158
Gene Symbol: HMGCS2
HMGCS2 		3-hydroxy-3-methylglutaryl-CoA synthase 2 0.666 0.577 4.3E-14
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 3158
Gene Symbol: HMGCS2
HMGCS2 		3-hydroxy-3-methylglutaryl-CoA synthase 2 0.666 0.577 4.3E-14
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 201562
Gene Symbol: HACD2
HACD2 		3-hydroxyacyl-CoA dehydratase 2 7.0E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		phenotype 0.100 None 1.000 2 2 2019 2019
Entrez Id: 201562
Gene Symbol: HACD2
HACD2 		3-hydroxyacyl-CoA dehydratase 2 7.0E-02
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 51495
Gene Symbol: HACD3
HACD3 		3-hydroxyacyl-CoA dehydratase 3 0.861 0.154 9.3E-03
CUI: C0021704
Disease: Intelligence
Intelligence 		phenotype 0.100 None 1.000 1 1 2019 2019