Variant (rsID / SNP)
rs17007666
rs17007666 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALK. Location: chromosome 2, position 29,419,473. Clinical significance in the table: Benign.
Reference-table entries
ALKBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:29419473
- Cytoband
- 2p23.2
- HGVS
- NM_004304.5(ALK):c.4164+163T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.