Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counseling. 21150883

2011
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK. 21325014

2011
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Novel and recurrent p14 mutations in Italian familial melanoma. 20132244

2010
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma families. 18981015

2008
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma. 15937071

2006
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample. 16234564

2005
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Geographical variation in the penetrance of CDKN2A mutations for melanoma. 12072543

2002
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden). 10956390

2000