Variant (rsID / SNP)
rs3829261
rs3829261 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CBL. Location: chromosome 11, position 119,176,499. Clinical significance in the table: Benign.
Reference-table entries
CBLBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:119176499
- Cytoband
- 11q23.3
- HGVS
- NM_005188.4(CBL):c.*6008T>C
- Allele change
- Silent
Associated conditions / phenotypes
CBL-related disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.