Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34886500
rs34886500
CDKN2A
CUI: C0025202
Disease: melanoma
melanoma 		0.010 GeneticVariation BEFREE Nucleotide-sequence analysis identified a single point mutation leading to a substitution of leucine for proline in codon 48 of exon 1 in a family with a history of melanoma and several other cancers. 9168184

1997