Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2363956
rs2363956
0.720 GeneticVariation BEFREE Additionally, rs4849887 was significantly associated with overall BC risk, and both rs2363956 and rs13000023 were associated with TNBC-specific risk, although none as strongly as the Duffy-null variant. 31356281

2019

dbSNP: rs2363956
rs2363956
C 0.720 GeneticVariation GWASCAT Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer. 24325915

2014

dbSNP: rs2363956
rs2363956
0.720 GeneticVariation BEFREE The five SNPs were also associated with triple-negative breast cancer in a separate study of 2,301 triple-negative cases and 3,949 controls (P(trend) = 1 × 10⁻⁷) to P(trend) = 8 × 10⁻⁵; rs2363956 per-allele OR = 0.80, 95% CI 0.74-0.87, P(trend) = 1.1 × 10⁻⁷ 20852631

2010

dbSNP: rs10069690
rs10069690
A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer. 24325915

2014

dbSNP: rs10771399
rs10771399
G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer. 24325915

2014

dbSNP: rs863225441
rs863225441
C 0.700 GeneticVariation CLINVAR

dbSNP: rs4987188
rs4987188
0.020 GeneticVariation BEFREE Structural debilitation of mutation G322D associated with MSH2 and their role in triple negative breast cancer. 30806579

2020

dbSNP: rs11540652
rs11540652
0.020 GeneticVariation BEFREE Transcriptome profiling identified ADORA2B as up-regulated in basal-like TNBC cell lines with R248Q-mutated TP53, with shRNA-screening suggesting the potential for a synthetic-lethal interaction between these genes. 30349649

2018

dbSNP: rs861539
rs861539
0.020 GeneticVariation BEFREE XRCC3 rs861539 TT is a potential predictive marker for TNBC in Taiwanese women and investigations in other populations are warranted for further universal application in cancer detection and prediction. 26543082

2016

dbSNP: rs11540652
rs11540652
0.020 GeneticVariation BEFREE This study supports using the biological markers of high expression of mtp53 R273H or R248Q as additional diagnostics for TNBC resistant subtypes often found in the AA community. 26703669

2015

dbSNP: rs4987188
rs4987188
0.020 GeneticVariation BEFREE The Gly322Asp polymorphism of the hMSH2 gene may be linked with TNBC occurrence in Polish women. 25134804

2015

dbSNP: rs861539
rs861539
0.020 GeneticVariation BEFREE In conclusion, XRCC2 Arg188His and XRCC3 Thr241Met polymorphisms may be regarded as predictive factors of triple-negative breast cancer in female population. 24728564

2015

dbSNP: rs8170
rs8170
0.020 GeneticVariation BEFREE In addition, a combined analysis of triple-negative cases from BCAC and the Triple Negative Breast Cancer Consortium (TNBCC; N = 3,566) identified a genome-wide significant association between rs8170 and triple-negative breast cancer risk (OR, 1.25; 95% CI, 1.18-1.33; P = 3.31 × 10(-13)]. 22331459

2012

dbSNP: rs8170
rs8170
0.020 GeneticVariation BEFREE We identified six single-nucleotide polymorphisms, including rs2046210 (ESR1), rs12662670 (ESR1), rs3803662 (TOX3), rs999737 (RAD51L1), rs8170 (19p13.1), and rs8100241 (19p13.1), significantly associated with the risk of triple-negative breast cancer. 21844186

2011

dbSNP: rs1042522
rs1042522
0.010 GeneticVariation BEFREE In conclusion, genetic variants in <i>TP53</i> were found in all TNBC tumors, with rs1042522 being the most frequent (94% of TNBC biopsies), which had not been previously reported in TNBC. 30867801

2019

dbSNP: rs13000023
rs13000023
0.010 GeneticVariation BEFREE Additionally, rs4849887 was significantly associated with overall BC risk, and both rs2363956 and rs13000023 were associated with TNBC-specific risk, although none as strongly as the Duffy-null variant. 31356281

2019

dbSNP: rs141366047
rs141366047
0.010 GeneticVariation BEFREE To assess the context-dependent roles, we carried out MDM2 and MDMX knockdown in orthotopic tumors of TNBC MDA-MB-231 cells expressing mtp53 R280K and MDM2 knockdown in ERα<sup>+</sup> T47D cells expressing mtp53 L194F. 30642351

2019

dbSNP: rs148047459
rs148047459
0.010 GeneticVariation BEFREE To assess the context-dependent roles, we carried out MDM2 and MDMX knockdown in orthotopic tumors of TNBC MDA-MB-231 cells expressing mtp53 R280K and MDM2 knockdown in ERα<sup>+</sup> T47D cells expressing mtp53 L194F. 30642351

2019

dbSNP: rs2491231
rs2491231
0.010 GeneticVariation BEFREE The rs2491231 variant in the <i>FLT3</i> gene was identified in 84% (16/19) of the samples, which not yet reported for TNBC, to the best of our knowledge. 30867801

2019

dbSNP: rs2814778
rs2814778
0.010 GeneticVariation BEFREE Frequency of the Duffy-null allele (rs2814778; an African ancestral variant adopted under selective pressure as protection against malaria) was associated with TNBC-specific risk (P < 0.0001), quantified West African Ancestry (P < 0.0001) and was more common in AA, Ghanaians, and TNBC cases. 31356281

2019

dbSNP: rs40239
rs40239
MET
0.010 GeneticVariation BEFREE <b>Conclusion:</b> Our case-control study suggests that MET T1010I seems to be a risk factor for TNBC in the Caucasian Greek population, in contrast with MET rs40239, where no correlation was found. 31213837

2019

dbSNP: rs4849887
rs4849887
0.010 GeneticVariation BEFREE Additionally, rs4849887 was significantly associated with overall BC risk, and both rs2363956 and rs13000023 were associated with TNBC-specific risk, although none as strongly as the Duffy-null variant. 31356281

2019

dbSNP: rs4938723
rs4938723
0.010 GeneticVariation BEFREE Prognostic significance of miR-34 rs4938723 T > C polymorphism in triple negative breast cancer patients. 30935968

2019

dbSNP: rs56391007
rs56391007
MET
0.010 GeneticVariation BEFREE <b>Conclusion:</b> Our case-control study suggests that MET T1010I seems to be a risk factor for TNBC in the Caucasian Greek population, in contrast with MET rs40239, where no correlation was found. 31213837

2019

dbSNP: rs769772228
rs769772228
0.010 GeneticVariation BEFREE To assess the context-dependent roles, we carried out MDM2 and MDMX knockdown in orthotopic tumors of TNBC MDA-MB-231 cells expressing mtp53 R280K and MDM2 knockdown in ERα<sup>+</sup> T47D cells expressing mtp53 L194F. 30642351

2019