Gene: CDKN2A ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894094
rs104894094
CDKN2A
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894097
rs104894097
CDKN2A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501263
rs1060501263
CDKN2A
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131691188
rs1131691188
CDKN2A
GC 0.700 CausalMutation CLINVAR

dbSNP: rs141798398
rs141798398
CDKN2A
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554653976
rs1554653976
CDKN2A
ACGGG 0.700 CausalMutation CLINVAR

dbSNP: rs1554659198
rs1554659198
CDKN2A ; CDKN2B-AS1
C 0.700 CausalMutation CLINVAR

dbSNP: rs36204594
rs36204594
CDKN2A
T 0.700 GeneticVariation CLINVAR

dbSNP: rs387906410
rs387906410
CDKN2A
AG 0.700 CausalMutation CLINVAR

dbSNP: rs398123152
rs398123152
CDKN2A
GC 0.700 CausalMutation CLINVAR

dbSNP: rs587780668
rs587780668
CDKN2A
AGGCTCCATGCTGCTCCCCGCCGCC 0.700 GeneticVariation CLINVAR

dbSNP: rs730881672
rs730881672
CDKN2A
AGCC 0.700 CausalMutation CLINVAR

dbSNP: rs749714198
rs749714198
CDKN2A
A 0.700 GeneticVariation CLINVAR

dbSNP: rs754806883
rs754806883
CDKN2A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs876658220
rs876658220
CDKN2A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs876658511
rs876658511
CDKN2A
G 0.700 CausalMutation CLINVAR

dbSNP: rs878853647
rs878853647
CDKN2A
G 0.700 CausalMutation CLINVAR

dbSNP: rs199907548
rs199907548
CDKN2A
G 0.700 GeneticVariation CLINVAR p16 proteins from melanoma-prone families are deficient in binding to Cdk4. 7566978

1995
dbSNP: rs559848002
rs559848002
CDKN2A
C 0.700 GeneticVariation CLINVAR p16 proteins from melanoma-prone families are deficient in binding to Cdk4. 7566978

1995
dbSNP: rs104894095
rs104894095
CDKN2A
G 0.700 CausalMutation CLINVAR Genetic discrimination and health insurance: an urgent need for reform. 7569991

1995
dbSNP: rs730881674
rs730881674
CDKN2A
C 0.700 CausalMutation CLINVAR CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families. 7640518

1995
dbSNP: rs104894098
rs104894098
CDKN2A
T 0.700 CausalMutation CLINVAR Mutations associated with familial melanoma impair p16INK4 function. 7647780

1995
dbSNP: rs199907548
rs199907548
CDKN2A
G 0.700 GeneticVariation CLINVAR Mutations associated with familial melanoma impair p16INK4 function. 7647780

1995
dbSNP: rs559848002
rs559848002
CDKN2A
C 0.700 GeneticVariation CLINVAR Mutations associated with familial melanoma impair p16INK4 function. 7647780

1995
dbSNP: rs730881675
rs730881675
CDKN2A
G 0.700 CausalMutation CLINVAR Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds. 7670475

1995