Variant (rsID / SNP)
rs2229071
rs2229071 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABL1. Location: chromosome 9, position 133,760,106. Clinical significance in the table: Benign.
Reference-table entries
ABL1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:133760106
- Cytoband
- 9q34.12
- HGVS
- NM_005157.6(ABL1):c.2429C>T (p.Pro810Leu)
- Allele change
- Missense_P829L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.