Variant (rsID / SNP)

rs104894095

rs104894095 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDKN2A. Location: chromosome 9, position 21,971,199. Clinical significance in the table: Pathogenic.

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Reference-table entries

CDKN2APathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 9:21971199
Cytoband: 9p21.3
HGVS: NM_000077.5(CDKN2A):c.159G>C (p.Met53Ile)
Allele change: Missense_M53I

Associated conditions / phenotypes

Melanoma, cutaneous malignant, susceptibility to, 2|Hereditary cancer-predisposing syndrome|Familial melanoma

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.