Variant (rsID / SNP)

rs35228363

rs35228363 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALK. Location: chromosome 2, position 29,497,967. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ALKBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:29497967
Cytoband: 2p23.2
HGVS: NM_004304.5(ALK):c.2039C>T (p.Thr680Ile)
Allele change: Missense_T680I

Associated conditions / phenotypes

Neuroblastoma, susceptibility to, 3|Hereditary cancer-predisposing syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.