Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0007114
Disease: Malignant neoplasm of skin
Malignant neoplasm of skin
0.340 GeneticVariation disease BEFREE EPHX1 Tyr113His, XPD C156A, and GSTT1 null genotypes were associated with skin cancer risk (OR = 2.99, 95% CI = 1.01-8.83; OR = 2.04, 95% CI = 0.99-4.27; OR = 1.74, 95% CI = 1.00-3.02, resp.). 26295053 2015
CUI: C0007114
Disease: Malignant neoplasm of skin
Malignant neoplasm of skin
0.340 Biomarker disease CTD_human EPHX1 Tyr113His, XPD C156A, and GSTT1 null genotypes were associated with skin cancer risk (OR = 2.99, 95% CI = 1.01-8.83; OR = 2.04, 95% CI = 0.99-4.27; OR = 1.74, 95% CI = 1.00-3.02, resp.). 26295053 2015
CUI: C0007114
Disease: Malignant neoplasm of skin
Malignant neoplasm of skin
0.340 GeneticVariation disease BEFREE Overall, the GSTT1 null genotype was not associated with the risk of skin cancer (OR, 1.01; 95 % CI 0.93-1.11; P = 0.76). 23184764 2013
CUI: C0007114
Disease: Malignant neoplasm of skin
Malignant neoplasm of skin
0.340 GeneticVariation disease BEFREE Several human GSTs, including GSTM1 and GSTT1, are polymorphic, and null polymorphisms have been associated with increased UVB erythemal sensitivity and skin cancer risk.PUVA also increases skin cancer risk. 21967523 2012
CUI: C0007114
Disease: Malignant neoplasm of skin
Malignant neoplasm of skin
0.340 GeneticVariation disease BEFREE GSTM1 and GSTT1 are deleted in approximately 50 and 20% of the Caucasian population, respectively, and GST null genotype has been associated with increased sunburn sensitivity and reduced minimal erythemal dose (MED) after broadband UVR exposure in healthy volunteers and with susceptibility to skin cancer. 20802377 2011