Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554653960
rs1554653960
CDKN2A
CUI: C0025202
Disease: melanoma
melanoma 		0.010 GeneticVariation BEFREE We have identified two novel CDKN2 mutations (88delG and Ala118Thr) which are likely to be associated with the development of melanoma, because of their co-segregation with the disease and their likely functional effect on the CDKN2 protein. 9328469

1997