Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060501262
rs1060501262
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501263
rs1060501263
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501265
rs1060501265
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554653915
rs1554653915
CGCATC 0.700 GeneticVariation CLINVAR

dbSNP: rs1554654052
rs1554654052
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554656624
rs1554656624
G 0.700 CausalMutation CLINVAR

dbSNP: rs1563888944
rs1563888944
GCT 0.700 GeneticVariation CLINVAR

dbSNP: rs1563889847
rs1563889847
GT 0.700 CausalMutation CLINVAR

dbSNP: rs398123152
rs398123152
GC 0.700 CausalMutation CLINVAR

dbSNP: rs786204195
rs786204195
T 0.700 CausalMutation CLINVAR

dbSNP: rs876658534
rs876658534
AA 0.700 GeneticVariation CLINVAR

dbSNP: rs876660436
rs876660436
C 0.700 CausalMutation CLINVAR

dbSNP: rs878853644
rs878853644
A 0.700 GeneticVariation CLINVAR

dbSNP: rs754806883
rs754806883
G 0.700 GeneticVariation CLINVAR The premaxilla and the ancestry of man. 20340316

1947

dbSNP: rs754806883
rs754806883
G 0.700 GeneticVariation CLINVAR Dietary habits, health beliefs, and food practices of elderly Chinese women. 2319082

1990

dbSNP: rs878853647
rs878853647
G 0.710 CausalMutation CLINVAR Germline p16 mutations in familial melanoma. 7987387

1994

dbSNP: rs121913387
rs121913387
A 0.700 CausalMutation CLINVAR Germline p16 mutations in familial melanoma. 7987387

1994

dbSNP: rs1563889584
rs1563889584
C 0.700 GeneticVariation CLINVAR Germline p16 mutations in familial melanoma. 7987387

1994

dbSNP: rs559848002
rs559848002
C 0.700 GeneticVariation CLINVAR Germline p16 mutations in familial melanoma. 7987387

1994

dbSNP: rs730881675
rs730881675
G 0.700 CausalMutation CLINVAR Rarity of somatic and germline mutations of the cyclin-dependent kinase 4 inhibitor gene, CDK4I, in melanoma. 7923152

1994

dbSNP: rs749714198
rs749714198
A 0.700 GeneticVariation CLINVAR Germline p16 mutations in familial melanoma. 7987387

1994

dbSNP: rs104894098
rs104894098
T 0.710 CausalMutation CLINVAR Mutations associated with familial melanoma impair p16INK4 function. 7647780

1995

dbSNP: rs104894095
rs104894095
T 0.700 CausalMutation CLINVAR Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds. 8595405

1995

dbSNP: rs104894095
rs104894095
G 0.700 CausalMutation CLINVAR Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds. 8595405

1995

dbSNP: rs104894097
rs104894097
G 0.700 CausalMutation CLINVAR Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds. 8570179

1995