Variant (rsID / SNP)
rs1765223
rs1765223 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to YARS1. Location: chromosome 1, position 33,256,884. Clinical significance in the table: Benign.
Reference-table entries
YARS1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:33256884
- Cytoband
- 1p35.1
- HGVS
- NM_003680.4(YARS1):c.592-29G>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.