Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12998806
rs12998806
0.710 GeneticVariation BEFREE In addition, we confirmed SNP rs10069690 was the best indicator for ER-negative breast cancer at 5p15.33 (OR = 1.30; P = 2.4 × 10 − 10) and identified rs12998806 as the best indicator for ER-positive breast cancer at 2q35 (OR = 1.34; P = 2.2 × 10 − 8) for women of African ancestry. 28171663

2016

dbSNP: rs11251942
rs11251942
0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463

2019

dbSNP: rs12938141
rs12938141
0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463

2019

dbSNP: rs140538758
rs140538758
0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463

2019

dbSNP: rs4717568
rs4717568
0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463

2019

dbSNP: rs587150
rs587150
0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463

2019

dbSNP: rs62235635
rs62235635
0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463

2019

dbSNP: rs6938753
rs6938753
0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463

2019

dbSNP: rs7082321
rs7082321
0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463

2019

dbSNP: rs73370840
rs73370840
0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463

2019

dbSNP: rs79116769
rs79116769
0.700 GeneticVariation GWASCAT Genome-wide association study of germline variants and breast cancer-specific mortality. 30787463

2019

dbSNP: rs10941679
rs10941679
0.020 GeneticVariation BEFREE Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation. 27640304

2016

dbSNP: rs10941679
rs10941679
0.020 GeneticVariation BEFREE In addition, we find both rs4415084 and rs10941679 conferred significantly greater risks of ER-positive breast cancer than of ER-negative tumors. 24039999

2013

dbSNP: rs700518
rs700518
0.020 GeneticVariation BEFREE Genetic polymorphism at Val80 (rs700518) of the CYP19A1 gene is associated with aromatase inhibitor associated bone loss in women with ER + breast cancer. 23643682

2013

dbSNP: rs700518
rs700518
0.020 GeneticVariation BEFREE Because AI use results in severe estrogen deficiency that may lead to changes in body composition, the aim of this study was to determine the effect of the rs700518 polymorphism in the CYP19A1 gene on the changes in body composition among postmenopausal women who were treated with AIs for ER+ breast cancer. 26049585

2015

dbSNP: rs865686
rs865686
0.020 GeneticVariation BEFREE We recently identified a novel susceptibility variant, rs865686, for estrogen-receptor positive breast cancer at 9q31.2. 25652398

2015

dbSNP: rs865686
rs865686
0.020 GeneticVariation BEFREE 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium. 22859399

2012

dbSNP: rs10069690
rs10069690
0.010 GeneticVariation BEFREE In addition, we confirmed SNP rs10069690 was the best indicator for ER-negative breast cancer at 5p15.33 (OR = 1.30; P = 2.4 × 10 − 10) and identified rs12998806 as the best indicator for ER-positive breast cancer at 2q35 (OR = 1.34; P = 2.2 × 10 − 8) for women of African ancestry. 28171663

2016

dbSNP: rs1042522
rs1042522
0.010 GeneticVariation BEFREE Association of p53 genetic polymorphism (Arg72Pro) with estrogen receptor positive breast cancer risk in Japanese women. 15183535

2004

dbSNP: rs10771399
rs10771399
0.010 GeneticVariation BEFREE We identified three new breast cancer risk loci at 12p11 (rs10771399; P = 2.7 × 10(-35)), 12q24 (rs1292011; P = 4.3 × 10(-19)) and 21q21 (rs2823093; P = 1.1 × 10(-12)). rs10771399 was associated with similar relative risks for both estrogen receptor (ER)-negative and ER-positive breast cancer, whereas the other two loci were associated only with ER-positive disease. 22267197

2012

dbSNP: rs10822013
rs10822013
0.010 GeneticVariation BEFREE When stratified based on breast cancer subtype, our analyses revealed that three SNPs (rs981782, rs10759243 and rs704010) correlated with ER+ breast cancer, while another three (rs4973768, rs1432679 and rs10822013) correlated with ER- breast cancer. 27863437

2016

dbSNP: rs1131691014
rs1131691014
0.010 GeneticVariation BEFREE Association of p53 genetic polymorphism (Arg72Pro) with estrogen receptor positive breast cancer risk in Japanese women. 15183535

2004

dbSNP: rs121434592
rs121434592
0.010 GeneticVariation BEFREE Both assays are employed at centralized testing laboratories operating according to quality standards for prospective identification of the AKT1 E17K mutation in ER+ breast cancer patients in the context of a clinical trial evaluating the AKT inhibitor AZD5363 in combination with endocrine (fulvestrant) therapy. 28472036

2017

dbSNP: rs12443621
rs12443621
0.010 GeneticVariation BEFREE However, rs12443621 AG/GG genotypes were significantly associated with increased risk of ER positive breast cancer (OR = 1.38, 95% CI = 1.01-1.88), compared with homozygote AA. 20213080

2010

dbSNP: rs1292011
rs1292011
0.010 GeneticVariation BEFREE We identified three new breast cancer risk loci at 12p11 (rs10771399; P = 2.7 × 10(-35)), 12q24 (rs1292011; P = 4.3 × 10(-19)) and 21q21 (rs2823093; P = 1.1 × 10(-12)). rs10771399 was associated with similar relative risks for both estrogen receptor (ER)-negative and ER-positive breast cancer, whereas the other two loci were associated only with ER-positive disease. 22267197

2012