Variant (rsID / SNP)
rs2256740
rs2256740 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALK. Location: chromosome 2, position 29,455,267. Clinical significance in the table: Benign.
Reference-table entries
ALKBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:29455267
- Cytoband
- 2p23.2
- HGVS
- NM_004304.5(ALK):c.2535T>C (p.Gly845=)
- Allele change
- Synonymous_G845G
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Neuroblastoma, susceptibility to, 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.