Variant (rsID / SNP)
rs2298650
rs2298650 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CBL. Location: chromosome 11, position 119,155,618. Clinical significance in the table: Benign.
Reference-table entries
CBLBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:119155618
- Cytoband
- 11q23.3
- HGVS
- NM_005188.4(CBL):c.1432-61G>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.