Variant (rsID / SNP)

rs35073634

rs35073634 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALK. Location: chromosome 2, position 29,449,820. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ALKBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:29449820
Cytoband: 2p23.2
HGVS: NM_004304.5(ALK):c.3035C>T (p.Thr1012Met)
Allele change: Missense_T1012M

Associated conditions / phenotypes

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

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.