Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Neonatal encephalocardiomyopathy caused by mutations in VARS2. 27502409

2017
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Neonatal encephalocardiomyopathy caused by mutations in VARS2. 27502409

2017
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre. 27290639

2016
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre. 27290639

2016
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies. 25058219

2014
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies. 25058219

2014
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies. 24827421

2014
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies. 24827421

2014
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Mitochondrial aminoacyl-tRNA synthetases in human disease. 23433712

2013
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Mitochondrial aminoacyl-tRNA synthetases in human disease. 23433712

2013
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Human diseases with impaired mitochondrial protein synthesis. 21708121

2011
Entrez Id: 57176
Gene Symbol: VARS2
VARS2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Human diseases with impaired mitochondrial protein synthesis. 21708121

2011