Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1353702185
rs1353702185
0.010 GeneticVariation BEFREE We investigated the effects of the germ-line single nucleotide polymorphisms TP53 R72P (215G>C) and MDM2 SNP309 (-410T>G), and p53 protein expression in breast tumors on survival. 20021639

2009

dbSNP: rs587781858
rs587781858
0.010 GeneticVariation BEFREE We investigated the effects of the germ-line single nucleotide polymorphisms TP53 R72P (215G>C) and MDM2 SNP309 (-410T>G), and p53 protein expression in breast tumors on survival. 20021639

2009

dbSNP: rs753535070
rs753535070
0.010 GeneticVariation BEFREE The MUC1 568 A/G polymorphism strongly influences CA 15-3 levels in healthy women and women with either benign or malignant breast tumors. 19121298

2009

dbSNP: rs1056892
rs1056892
0.010 GeneticVariation BEFREE Another variant CBR3 730G>A was associated with higher doxorubicinol AUC (P=0.009, GG vs. AA) and CBR3 expression in breast tumor tissue (P=0.001, GG vs AA). 18551042

2008

dbSNP: rs1239905891
rs1239905891
0.010 GeneticVariation BEFREE The purposes of this study were to analyse the genotype of TGF-beta1 at T29C and TGF-beta1 phenotype in breast tumours, and to evaluate their associations with IGFs and clinical characteristics of breast cancer. 18827819

2008

dbSNP: rs1800470
rs1800470
0.010 GeneticVariation BEFREE The purposes of this study were to analyse the genotype of TGF-beta1 at T29C and TGF-beta1 phenotype in breast tumours, and to evaluate their associations with IGFs and clinical characteristics of breast cancer. 18827819

2008

dbSNP: rs35490896
rs35490896
0.010 GeneticVariation BEFREE A separate analysis of the CLSPN c.3839C>T (rs35490896) variant that was observed more frequently in breast tumors than in pancreatic tumors or normal controls failed to detect a significant association with breast cancer risk in a Mayo Clinic breast cancer case-control study. 18281469

2008

dbSNP: rs8133052
rs8133052
0.010 GeneticVariation BEFREE A common CBR3 11G>A variant was associated with lower doxorubicinol area under the concentration-time curve (AUC)/doxorubicin AUC metabolite ratio (P=0.009, GG vs. AA; trend test, P=0.004), lower CBR3 expression in breast tumor tissue (P=0.001, GG vs. AA), greater tumor reduction (P=0.015, GG vs. AA), and greater percentage reduction of leukocyte and platelet counts at nadir (trend test, P < or = 0.03). 18551042

2008

dbSNP: rs984257990
rs984257990
0.010 GeneticVariation BEFREE The purposes of this study were to analyse the genotype of TGF-beta1 at T29C and TGF-beta1 phenotype in breast tumours, and to evaluate their associations with IGFs and clinical characteristics of breast cancer. 18827819

2008

dbSNP: rs146312682
rs146312682
0.010 GeneticVariation BEFREE The rare Ser255Arg variant was identified in only sporadic breast tumors (2/165 tumors). 17889706

2007

dbSNP: rs28997576
rs28997576
0.010 GeneticVariation BEFREE Cys557Ser carriers, with or without the BRCA2 mutation, had an increased risk of subsequent primary breast tumors after the first breast cancer diagnosis compared to non-carriers. 16768547

2006

dbSNP: rs41293463
rs41293463
0.010 GeneticVariation BEFREE This association was much weaker with the same fragment bearing a missense mutation (M1775R) that has been identified in breast tumors. 10403822

1999

dbSNP: rs17879961
rs17879961
0.020 GeneticVariation BEFREE Our analyses suggest that there are fundamental differences in breast tumors of CHEK2:p.I157T and c.1100delC carriers. 27716369

2016

dbSNP: rs11249433
rs11249433
0.020 GeneticVariation BEFREE Our results in two independent data sets suggest that rs11249433, which is located between the NOTCH2 and FCGR1B genes within the 1p11.2 locus, is more strongly associated with risk of breast tumors with low or absent E-cadherin expression, and suggest that evaluation of E-cadherin tumor tissue expression may be useful in clarifying breast cancer risk factor associations. 24292867

2014

dbSNP: rs17879961
rs17879961
0.020 GeneticVariation BEFREE We found an even stronger significant association between the CHEK2 I157T C variant and increased risk of lobular type breast tumors (OR = 4.17, 95% CI = 2.89-6.03, P < 0.0001). 22799331

2012

dbSNP: rs11249433
rs11249433
0.020 GeneticVariation BEFREE This is the first study to show that the expression of NOTCH2 differs in subgroups of breast tumors and by genotypes of the breast cancer-associated SNP rs11249433. 20482849

2010

dbSNP: rs1131691014
rs1131691014
0.020 GeneticVariation BEFREE We investigated the effects of the germ-line single nucleotide polymorphisms TP53 R72P (215G>C) and MDM2 SNP309 (-410T>G), and p53 protein expression in breast tumors on survival. 20021639

2009

dbSNP: rs878854066
rs878854066
0.020 GeneticVariation BEFREE We investigated the effects of the germ-line single nucleotide polymorphisms TP53 R72P (215G>C) and MDM2 SNP309 (-410T>G), and p53 protein expression in breast tumors on survival. 20021639

2009

dbSNP: rs1131691014
rs1131691014
0.020 GeneticVariation BEFREE Our aim was to evaluate association of R72P with breast cancer risk as well as histopathologic features of the breast tumors and survival. 16033823

2005

dbSNP: rs878854066
rs878854066
0.020 GeneticVariation BEFREE Our aim was to evaluate association of R72P with breast cancer risk as well as histopathologic features of the breast tumors and survival. 16033823

2005

dbSNP: rs1042522
rs1042522
0.030 GeneticVariation BEFREE Taken together, we showed the preferential loss of the rs1042522 C allele, which is protective against BC progression, in breast tumors. 21810023

2011

dbSNP: rs1042522
rs1042522
0.030 GeneticVariation BEFREE We investigated the effects of the germ-line single nucleotide polymorphisms TP53 R72P (215G>C) and MDM2 SNP309 (-410T>G), and p53 protein expression in breast tumors on survival. 20021639

2009

dbSNP: rs1462893414
rs1462893414
0.030 GeneticVariation BEFREE These preliminary results suggest that OCs may interact with the ESR1 A908G mutant receptor to drive the development of some breast tumors. 17553133

2007

dbSNP: rs1462893414
rs1462893414
0.030 GeneticVariation BEFREE Consistent with our previous finding of this somatic ERalpha mutation in breast ductal hyperplasias, we now present evidence that the A908G mutation is present in invasive breast tumors using an optimized sequencing method. 17545528

2007

dbSNP: rs1042522
rs1042522
0.030 GeneticVariation BEFREE Our aim was to evaluate association of R72P with breast cancer risk as well as histopathologic features of the breast tumors and survival. 16033823

2005