Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060501260
rs1060501260
CDKN2A
A 0.700 GeneticVariation CLINVAR Classifying variants of CDKN2A using computational and laboratory studies. 21462282

2011
dbSNP: rs1060501260
rs1060501260
CDKN2A
A 0.700 GeneticVariation CLINVAR Multiple primary tumors as an indicator for p16INK4a germline mutations in pancreatic cancer patients? 11075991

2000
dbSNP: rs1060501260
rs1060501260
CDKN2A
A 0.700 GeneticVariation CLINVAR Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population. 8710906

1996