Gene entry
SARS2
seryl-tRNA synthetase 2, mitochondrial
- Chromosome
- 19
- Cytoband
- 19q13.2
- Variants (rsID)
- 9
SARS2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.2). Its official name is “seryl-tRNA synthetase 2, mitochondrial”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs34264048Benignsingle nucleotide variantHyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
- rs144760517Conflicting interpretationssingle nucleotide variantHyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
- rs200300920Conflicting interpretationssingle nucleotide variantHyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
- rs34050897Conflicting interpretationssingle nucleotide variantHyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
- rs370612303Conflicting interpretationssingle nucleotide variantHyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
- rs528674259Conflicting interpretationssingle nucleotide variantHyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
- rs145754412Pathogenicsingle nucleotide variantHyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
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.