Variant (rsID / SNP)
rs768966657
rs768966657 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDKN2A. Location: chromosome 9, position 21,971,020. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
CDKN2APathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- Duplication
- Chromosome / position
- 9:21971020
- Cytoband
- 9p21.3
- HGVS
- NM_000077.5(CDKN2A):c.335_337dup (p.Arg112dup)
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Familial melanoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.