Variant (rsID / SNP)
rs79339096
rs79339096 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALK. Location: chromosome 2, position 29,446,405. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
ALKConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:29446405
- Cytoband
- 2p23.2
- HGVS
- NM_004304.5(ALK):c.3173-11C>T
- Allele change
- Silent
Associated conditions / phenotypes
Neuroblastoma Susceptibility|Neuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.