Gene: CDKN2A ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs768966657
rs768966657
CDKN2A
AGAC 0.700 GeneticVariation CLINVAR Germline CDKN2A Mutation Status and Survival in Familial Melanoma Cases. 27287845

2016
dbSNP: rs104894095
rs104894095
CDKN2A
T 0.700 CausalMutation CLINVAR BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE study. 25356972

2015
dbSNP: rs104894097
rs104894097
CDKN2A
G 0.700 CausalMutation CLINVAR BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE study. 25356972

2015
dbSNP: rs104894097
rs104894097
CDKN2A
G 0.700 CausalMutation CLINVAR Novel CDKN2A mutations in Austrian melanoma patients. 26225579

2015
dbSNP: rs45476696
rs45476696
CDKN2A
A 0.700 CausalMutation CLINVAR BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE study. 25356972

2015
dbSNP: rs587780668
rs587780668
CDKN2A
AGGCTCCATGCTGCTCCCCGCCGCC 0.700 GeneticVariation CLINVAR Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition. 25803691

2015
dbSNP: rs587782083
rs587782083
CDKN2A ; CDKN2B-AS1
T 0.700 CausalMutation CLINVAR Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition. 25803691

2015
dbSNP: rs587782206
rs587782206
CDKN2A
G 0.700 CausalMutation CLINVAR Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition. 25803691

2015
dbSNP: rs768966657
rs768966657
CDKN2A
AGAC 0.700 GeneticVariation CLINVAR Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition. 25803691

2015
dbSNP: rs864622636
rs864622636
CDKN2A
A 0.700 CausalMutation CLINVAR BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE study. 25356972

2015
dbSNP: rs864622636
rs864622636
CDKN2A
A 0.700 CausalMutation CLINVAR Personalized genomic analyses for cancer mutation discovery and interpretation. 25877891

2015
dbSNP: rs104894095
rs104894095
CDKN2A
G 0.700 CausalMutation CLINVAR A short acidic motif in ARF guards against mitochondrial dysfunction and melanoma susceptibility. 25370744

2014
dbSNP: rs104894109
rs104894109
CDKN2A
A 0.700 CausalMutation CLINVAR A short acidic motif in ARF guards against mitochondrial dysfunction and melanoma susceptibility. 25370744

2014
dbSNP: rs1064794292
rs1064794292
CDKN2A
T 0.700 GeneticVariation CLINVAR CDKN2A unclassified variants in familial malignant melanoma: combining functional and computational approaches for their assessment. 24659262

2014
dbSNP: rs121913387
rs121913387
CDKN2A
A 0.700 CausalMutation CLINVAR A short acidic motif in ARF guards against mitochondrial dysfunction and melanoma susceptibility. 25370744

2014
dbSNP: rs1554653956
rs1554653956
CDKN2A
T 0.700 GeneticVariation CLINVAR Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom. 25780468

2014
dbSNP: rs587782083
rs587782083
CDKN2A ; CDKN2B-AS1
T 0.700 CausalMutation CLINVAR [CDKN2A-mutation in a family with hereditary malignant melanoma]. 25294512

2014
dbSNP: rs754806883
rs754806883
CDKN2A
G 0.700 GeneticVariation CLINVAR Genotype analysis in Hungarian patients with multiple primary melanoma. 24660985

2014
dbSNP: rs768966657
rs768966657
CDKN2A
AGAC 0.700 GeneticVariation CLINVAR High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families. 24935963

2014
dbSNP: rs104894097
rs104894097
CDKN2A
G 0.700 CausalMutation CLINVAR Familial melanoma-associated mutations in p16 uncouple its tumor-suppressor functions. 23190892

2013
dbSNP: rs749714198
rs749714198
CDKN2A
A 0.700 GeneticVariation CLINVAR Familial melanoma-associated mutations in p16 uncouple its tumor-suppressor functions. 23190892

2013
dbSNP: rs104894099
rs104894099
CDKN2A
C 0.700 CausalMutation CLINVAR Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family. 22841127

2012
dbSNP: rs104894109
rs104894109
CDKN2A
A 0.700 CausalMutation CLINVAR Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family. 22841127

2012
dbSNP: rs1060501266
rs1060501266
CDKN2A
C 0.700 GeneticVariation CLINVAR Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family. 22841127

2012
dbSNP: rs199907548
rs199907548
CDKN2A
C 0.700 GeneticVariation CLINVAR Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family. 22841127

2012