Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
0.020 | GeneticVariation | BEFREE | The present study aimed to examine the frequency of chromosomal aberrations and the mitotic index in patients with chronic hepatitis B and their possible association with p53 gene exon 4 codon 72 Arg72Pro (Ex4+119 G>C; rs1042522) polymorphism. | 22892830 | 2012 |
||||
|
0.020 | GeneticVariation | BEFREE | The present study aimed to examine the frequency of chromosomal aberrations and the mitotic index in patients with chronic hepatitis B and their possible association with p53 gene exon 4 codon 72 Arg72Pro (Ex4+119 G>C; rs1042522) polymorphism. | 22892830 | 2012 |
||||
|
0.020 | GeneticVariation | BEFREE | The present study aimed to examine the frequency of chromosomal aberrations and the mitotic index in patients with chronic hepatitis B and their possible association with p53 gene exon 4 codon 72 Arg72Pro (Ex4+119 G>C; rs1042522) polymorphism. | 22892830 | 2012 |
||||
|
0.020 | GeneticVariation | BEFREE | In conclusion, the TP53 gene Arg72Pro polymorphism appreciably influence on occurrence of chromosome aberrations</span> in cancer. | 20512840 | 2010 |
||||
|
0.020 | GeneticVariation | BEFREE | In conclusion, the TP53 gene Arg72Pro polymorphism appreciably influence on occurrence of chromosome aberrations</span> in cancer. | 20512840 | 2010 |
||||
|
0.020 | GeneticVariation | BEFREE | In conclusion, the TP53 gene Arg72Pro polymorphism appreciably influence on occurrence of chromosome aberrations</span> in cancer. | 20512840 | 2010 |
||||
|
0.010 | GeneticVariation | BEFREE | We infer that U2AF1 S34 mutations characterize a distinct subgroup of MDS: younger age of onset and differential associations with particular cytogenetic aberrations depending on specific mutations [S34Y to +8; S34F to +8 and del(20q)]. | 28938223 | 2017 |
||||
|
0.010 | GeneticVariation | BEFREE | We infer that U2AF1 S34 mutations characterize a distinct subgroup of MDS: younger age of onset and differential associations with particular cytogenetic aberrations depending on specific mutations [S34Y to +8; S34F to +8 and del(20q)]. | 28938223 | 2017 |