Variant (rsID / SNP)
rs2270004
rs2270004 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARS2. Location: chromosome 1, position 55,224,131. Clinical significance in the table: Benign.
Reference-table entries
PARS2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:55224131
- Cytoband
- 1p32.3
- HGVS
- NM_152268.4(PARS2):c.704A>G (p.Asn235Ser)
- Allele change
- Missense_N235S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.