Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 GeneticVariation group CLINVAR Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population. 8710906 1996
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 GeneticVariation group CLINVAR Functional reassessment of P16 variants using a transfection-based assay. 10389768 1999
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 GeneticVariation group CLINVAR Estimating the relative risk of developing melanoma in INK4A carriers. 15075790 2004
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Genotype-phenotype relationships in U.S. melanoma-prone families with CDKN2A and CDK4 mutations. 10861313 2000
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Indication for CDKN2A-mutation analysis in familial pancreatic cancer families without melanomas. 22636603 2012
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Functional analysis of CDKN2A/p16INK4a 5'-UTR variants predisposing to melanoma. 20093296 2010
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 GeneticVariation group CLINVAR Biologic and biochemical analyses of p16(INK4a) mutations from primary tumors. 10491434 1999
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Multiple primary melanomas in a CDKN2A mutation carrier exposed to ionizing radiation. 18025365 2007
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study. 20876876 2010
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Mutation screening of the CDKN2A promoter in melanoma families. 10738302 2000
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 GeneticVariation group CLINVAR Novel CDKN2A mutations detected in western Swedish families with hereditary malignant melanoma. 17255954 2007
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 GeneticVariation group CLINVAR The missing puzzle piece: splicing mutations. 24294354 2013
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 GeneticVariation group CLINVAR A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families. 12700603 2003
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Germline CDKN2A Mutation Status and Survival in Familial Melanoma Cases. 27287845 2016
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 GeneticVariation group CLINVAR Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family. 22841127 2012
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Familial melanoma-associated mutations in p16 uncouple its tumor-suppressor functions. 23190892 2013
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas. 9699728 1998
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer. 21614589 2011
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 GeneticVariation group CLINVAR Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A. 20340136 2010
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition. 25803691 2015
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds. 8595405 1995
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 GeneticVariation group CLINVAR Analysis of p16INK4a and its interaction with CDK4. 8573142 1996
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families. 7640518 1995
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Prospective risk of cancer and the influence of tobacco use in carriers of the p16-Leiden germline variant. 25227142 2015
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.110 CausalMutation group CLINVAR Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group. 9425228 1998