Source: CLINGEN

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: 80704
Gene Symbol: SLC19A3
SLC19A3 		solute carrier family 19 member 3 0.610 0.692 0.10
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		disease 0.340 definitive 1.000 10 0 2010 2017
Entrez Id: 80704
Gene Symbol: SLC19A3
SLC19A3 		solute carrier family 19 member 3 0.610 0.692 0.10
CUI: C1838951
Disease: LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY 		disease 0.300 definitive 1.000 10 0 2010 2016
Entrez Id: 80704
Gene Symbol: SLC19A3
SLC19A3 		solute carrier family 19 member 3 0.610 0.692 0.10
CUI: C1850597
Disease: Leigh Syndrome Due To Mitochondrial Complex II Deficiency
Leigh Syndrome Due To Mitochondrial Complex II Deficiency 		disease 0.300 definitive 1.000 10 0 2010 2016
Entrez Id: 80704
Gene Symbol: SLC19A3
SLC19A3 		solute carrier family 19 member 3 0.610 0.692 0.10
CUI: C1850598
Disease: Leigh Syndrome due to Mitochondrial Complex III Deficiency
Leigh Syndrome due to Mitochondrial Complex III Deficiency 		disease 0.300 definitive 1.000 10 0 2010 2016
Entrez Id: 80704
Gene Symbol: SLC19A3
SLC19A3 		solute carrier family 19 member 3 0.610 0.692 0.10
CUI: C1850599
Disease: Leigh Syndrome due to Mitochondrial Complex IV Deficiency
Leigh Syndrome due to Mitochondrial Complex IV Deficiency 		disease 0.300 definitive 1.000 10 0 2010 2016
Entrez Id: 80704
Gene Symbol: SLC19A3
SLC19A3 		solute carrier family 19 member 3 0.610 0.692 0.10
CUI: C1850600
Disease: Leigh Syndrome due to Mitochondrial Complex V Deficiency
Leigh Syndrome due to Mitochondrial Complex V Deficiency 		disease 0.300 definitive 1.000 10 0 2010 2016
Entrez Id: 80704
Gene Symbol: SLC19A3
SLC19A3 		solute carrier family 19 member 3 0.610 0.692 0.10
CUI: C2931891
Disease: Necrotizing encephalopathy, infantile subacute, of Leigh
Necrotizing encephalopathy, infantile subacute, of Leigh 		disease 0.300 definitive 1.000 10 0 2010 2016