Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs749714198
rs749714198
CDKN2A
CUI: C1838547
Disease: MELANOMA-PANCREATIC CANCER SYNDROME
MELANOMA-PANCREATIC CANCER SYNDROME 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs749714198
rs749714198
CDKN2A
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs747621669
rs747621669
CDKN2A
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.700 GeneticVariation UNIPROT

dbSNP: rs730881672
rs730881672
CDKN2A
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		AGCC 0.700 CausalMutation CLINVAR

dbSNP: rs6413464
rs6413464
CDKN2A
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs6413463
rs6413463
CDKN2A
CUI: C0023418
Disease: leukemia
leukemia 		0.700 GeneticVariation UNIPROT

dbSNP: rs587780668
rs587780668
CDKN2A
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		AGGCTCCATGCTGCTCCCCGCCGCC 0.700 GeneticVariation CLINVAR

dbSNP: rs587780668
rs587780668
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		AGGCTCCATGCTGCTCCCCGCCGCC 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs587776716
rs587776716
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs587776716
rs587776716
CDKN2A
CUI: C1838547
Disease: MELANOMA-PANCREATIC CANCER SYNDROME
MELANOMA-PANCREATIC CANCER SYNDROME 		A 0.700 CausalMutation CLINVAR

dbSNP: rs398123152
rs398123152
CDKN2A
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		GC 0.700 CausalMutation CLINVAR

dbSNP: rs398123152
rs398123152
CDKN2A
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma 		GC 0.700 CausalMutation CLINVAR

dbSNP: rs387906410
rs387906410
CDKN2A
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		AG 0.700 CausalMutation CLINVAR

dbSNP: rs387906410
rs387906410
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		AG 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs372266620
rs372266620
CDKN2A
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs36204594
rs36204594
CDKN2A
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs36204594
rs36204594
CDKN2A
CUI: C0025202
Disease: melanoma
melanoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs199907548
rs199907548
CDKN2A
CUI: C0005426
Disease: Biliary Tract Neoplasm
Biliary Tract Neoplasm 		0.700 GeneticVariation UNIPROT

dbSNP: rs1800586
rs1800586
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1800586
rs1800586
CDKN2A
CUI: C1835042
Disease: Melanoma astrocytoma syndrome
Melanoma astrocytoma syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1563889847
rs1563889847
CDKN2A
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma 		GT 0.700 CausalMutation CLINVAR

dbSNP: rs1563888944
rs1563888944
CDKN2A
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma 		GCT 0.700 GeneticVariation CLINVAR

dbSNP: rs1554659198
rs1554659198
CDKN2A ; CDKN2B-AS1
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1554656624
rs1554656624
CDKN2A
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1554654052
rs1554654052
CDKN2A
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma 		A 0.700 CausalMutation CLINVAR