Source: INFERRED

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: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		phenotype 0.100 None 1.000 1 1 2011 2011
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0596887
Disease: mathematical ability
mathematical ability 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		phenotype 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		phenotype 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		group 0.100 None 1.000 1 1 2011 2011
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0005890
Disease: Body Height
Body Height 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		group 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		phenotype 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0013595
Disease: Eczema
Eczema 		disease 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		group 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		phenotype 0.100 None 1.000 1 1 2011 2011
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0011847
Disease: Diabetes
Diabetes 		disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0042834
Disease: Vital capacity
Vital capacity 		phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0037369
Disease: Smoking
Smoking 		phenotype 0.100 None 1.000 1 1 2017 2017
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		disease 0.100 None 1.000 1 1 2019 2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		group 0.100 None 1.000 1 1 2016 2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		phenotype 0.100 None 0 0
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8 		solute carrier family 39 member 8 0.584 0.769 0.67
CUI: C1849937
Disease: Disproportionate short-limb short stature
Disproportionate short-limb short stature 		phenotype 0.100 None 0 0