Variant (rsID / SNP)
rs115720584
rs115720584 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TARS2. Location: chromosome 1, position 150,470,061. Clinical significance in the table: Benign.
Reference-table entries
TARS2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:150470061
- Cytoband
- 1q21.2
- HGVS
- NM_025150.5(TARS2):c.1076C>T (p.Thr359Met)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.