Gene entry
PARS2
prolyl-tRNA synthetase 2, mitochondrial
- Chromosome
- 1
- Cytoband
- 1p32.3
- Variants (rsID)
- 5
PARS2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p32.3). Its official name is “prolyl-tRNA synthetase 2, mitochondrial”. The reference table lists 5 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs11577368Benignsingle nucleotide variant
- rs116816976Benignsingle nucleotide variant
- rs2270004Benignsingle nucleotide variant
- rs35201073Conflicting interpretationssingle nucleotide variantDevelopmental and epileptic encephalopathy, 75
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.