Gene entry
VARS2
valyl-tRNA synthetase 2, mitochondrial
- Chromosome
- 6
- Cytoband
- 6p21.33
- Variants (rsID)
- 33
VARS2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p21.33). Its official name is “valyl-tRNA synthetase 2, mitochondrial”. The reference table lists 33 variants (rsID) for this gene.
Clinically classified variants
12 reference-table entries with clinical significance.
- rs1043483Benignsingle nucleotide variantCombined oxidative phosphorylation defect type 20
- rs1264301Benignsingle nucleotide variant
- rs17189635Benignsingle nucleotide variant
- rs2074506Benignsingle nucleotide variantCombined oxidative phosphorylation defect type 20
- rs2249464Benignsingle nucleotide variantCombined oxidative phosphorylation defect type 20
- rs4678Benignsingle nucleotide variant
- rs61746524Benignsingle nucleotide variant
- rs6926224Benignsingle nucleotide variant
- rs6926723Benignsingle nucleotide variant
- rs753725Benignsingle nucleotide variantCombined oxidative phosphorylation defect type 20
- rs9394021Benignsingle nucleotide variantCombined oxidative phosphorylation defect type 20
- rs138855624Conflicting interpretationssingle nucleotide variantCombined oxidative phosphorylation defect type 20
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
