Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878853647
rs878853647
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		G 0.800 CausalMutation CLINVAR

dbSNP: rs137854599
rs137854599
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		T 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs137854597
rs137854597
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		T 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs113798404
rs113798404
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		G 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs113798404
rs113798404
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		0.800 GeneticVariation UNIPROT

dbSNP: rs104894099
rs104894099
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		C 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs104894098
rs104894098
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		T 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs104894097
rs104894097
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		G 0.800 CausalMutation CLINVAR

dbSNP: rs104894097
rs104894097
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		G 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs104894095
rs104894095
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		G 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs104894094
rs104894094
CDKN2A
CUI: C0025202
Disease: melanoma
melanoma 		A 0.800 CausalMutation CLINVAR

dbSNP: rs104894094
rs104894094
CDKN2A
CUI: C1835044
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 		A 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs104894097
rs104894097
CDKN2A
CUI: C0025202
Disease: melanoma
melanoma 		G 0.750 CausalMutation CLINVAR

dbSNP: rs1064794292
rs1064794292
CDKN2A
CUI: C0025202
Disease: melanoma
melanoma 		0.710 GeneticVariation UNIPROT

dbSNP: rs878853647
rs878853647
CDKN2A
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		G 0.700 CausalMutation CLINVAR

dbSNP: rs878853644
rs878853644
CDKN2A
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs876660436
rs876660436
CDKN2A
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma 		C 0.700 CausalMutation CLINVAR

dbSNP: rs876658534
rs876658534
CDKN2A
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma 		AA 0.700 GeneticVariation CLINVAR

dbSNP: rs876658511
rs876658511
CDKN2A
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		G 0.700 CausalMutation CLINVAR

dbSNP: rs876658220
rs876658220
CDKN2A
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs786204195
rs786204195
CDKN2A
CUI: C1512419
Disease: Hereditary Melanoma
Hereditary Melanoma 		T 0.700 CausalMutation CLINVAR

dbSNP: rs760065045
rs760065045
CDKN2A
CUI: C0005426
Disease: Biliary Tract Neoplasm
Biliary Tract Neoplasm 		0.700 GeneticVariation UNIPROT

dbSNP: rs757497674
rs757497674
CDKN2A
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs754806883
rs754806883
CDKN2A
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs754806883
rs754806883
CDKN2A
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		G 0.700 GeneticVariation CLINVAR