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Variant (rsID / SNP)

rs116150891

CDKN2A

rs116150891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDKN2A. Location: chromosome 9, position 21,970,928. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CDKN2ABenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
9:21970928
Cytoband
9p21.3
HGVS
NM_000077.5(CDKN2A):c.430C>T (p.Arg144Cys)
Allele change
Missense_R144C

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Melanoma-pancreatic cancer syndrome|Familial melanoma

Public references

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