6.1.1.9	Brain Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30755602&form=6&db=m	Biallelic mutations in valyl-tRNA synthetase gene VARS are associated with a progressive neurodevelopmental epileptic encephalopathy.	causal interaction,unassigned	3,0	
6.1.1.9	Brain Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30755616&form=6&db=m	Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish.	ongoing research,therapeutic application,unassigned	1,1,0	
6.1.1.9	Cardiomyopathy, Hypertrophic	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33937156&form=6&db=m	Case Report and Review of the Literature: A New and a Recurrent Variant in the VARS2 Gene Are Associated With Isolated Lethal Hypertrophic Cardiomyopathy, Hyperlactatemia, and Pulmonary Hypertension in Early Infancy.	causal interaction,unassigned	4,0	
6.1.1.9	Epilepsy	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30755616&form=6&db=m	Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish.	ongoing research,therapeutic application,unassigned	1,1,0	
6.1.1.9	Epilepsy	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33937156&form=6&db=m	Case Report and Review of the Literature: A New and a Recurrent Variant in the VARS2 Gene Are Associated With Isolated Lethal Hypertrophic Cardiomyopathy, Hyperlactatemia, and Pulmonary Hypertension in Early Infancy.	causal interaction,unassigned	4,0	
6.1.1.9	Infections	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=330535&form=6&db=m	Analysis of the structure of T4 bacteriophage-modified valyl-tRNA synthetase by limited proteolysis and isoelectric focusing.	therapeutic application,unassigned	2,0	
6.1.1.9	Infections	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3881597&form=6&db=m	Response of a phage modification factor to enhanced production of its target molecule.	unassigned	-	
6.1.1.9	Infections	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20668681&form=6&db=m	C. elegans germline-deficient mutants respond to pathogen infection using shared and distinct mechanisms.	causal interaction,diagnostic usage,therapeutic application,unassigned	1,3,2,0	
6.1.1.9	Leukemia	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=837925&form=6&db=m	Subcellular distribution of aminoacyl-tRNA synthetases in various eukaryotic cells.	diagnostic usage,unassigned	1,0	
6.1.1.9	Leukemia	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9461376&form=6&db=m	Evolutionary significance of intra-genome duplications on human chromosomes.	unassigned	-