Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. 25980754

2015

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children. 26104880

2015

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Genotype analysis in Hungarian patients with multiple primary melanoma. 24660985

2014

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom. 25780468

2014

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Classifying variants of CDKN2A using computational and laboratory studies. 21462282

2011

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK. 21325014

2011

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A. 20340136

2010

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients. 19260062

2009

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypes. 19484507

2009

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. 17047042

2006

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Structural basis for inhibition of the cyclin-dependent kinase Cdk6 by the tumour suppressor p16INK4a. 9751050

1998

dbSNP: rs372670098
rs372670098
C 0.700 GeneticVariation CLINVAR Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group. 9425228

1998