Variant (rsID / SNP)
rs35093491
rs35093491 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALK. Location: chromosome 2, position 29,543,736. Clinical significance in the table: Benign.
Reference-table entries
ALKBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:29543736
- Cytoband
- 2p23.2
- HGVS
- NM_004304.5(ALK):c.1427T>C (p.Val476Ala)
- Allele change
- Missense_V476A
Associated conditions / phenotypes
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.