Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879253942
rs879253942
TP53
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.040 GeneticVariation BEFREE MYD88 p.L265P and CD79B p.Y196C/H mutations were analyzed in diffuse large B-cell lymphoma (DLBCL) patients whose tumor samples were available (N = 29). 31436356

2019
dbSNP: rs879253942
rs879253942
TP53
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.040 GeneticVariation BEFREE The study included 232 HCC patients with folate nutrition, MTHFR C677T polymorphic, p53 genetic and tumour pathological data collected and analyzed for their survivals after a 7.8-years following up. 23996892

2014
dbSNP: rs879253942
rs879253942
TP53
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.040 GeneticVariation BEFREE MTHFR C677T was found to be a strong predictor of the presence of multifocal tumour (odds ratio, 4.1; 95% CI, 1.1-15.7; P=0.035). 20371218

2010
dbSNP: rs879253942
rs879253942
TP53
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.040 GeneticVariation BEFREE Liver metastases (n = 93) along with primary tumors (n = 48) were analyzed for K-Ras mutations (codons 12 and 13), p53 mutations (exons 4-9), p53 polymorphism (codon 72), thymidylate synthase (TS) polymorphism (28-bp repeats including G>C mutation), methylenetetrahydrofolate reductase polymorphism (677C>T, 1298A>C), thymidylate synthase (TS) activity, dihydropyrimidine dehydrogenase activity, folylpolyglutamate synthase activity, and p53 protein expression. 18676755

2008