Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3787268
rs3787268
0.020 GeneticVariation BEFREE In the genetic model analysis, the minor allele "T" of rs11225394 in MMP8 was associated with increased risk of BC under the recessive model (P = 0.019), and the minor allele "A" of rs</span>3787268 was associated with decreased risk of BC under the dominant model (P = 0.014). 30194384

2018

dbSNP: rs3787268
rs3787268
0.020 GeneticVariation BEFREE We found that the MMP9 rs3787268 GA+AA genotypes were significantly associated with poor DFS and DDFS of patients with breast cancer (log-rank p-values 0.045 and 0.028, respectively), especially in some subgroups of patients. 23570558

2013

dbSNP: rs3918249
rs3918249
0.010 GeneticVariation BEFREE Additionally, the haplotype "AGTCA" constructed by rs3740938, rs2012390, rs1940475, rs11225394, and rs11225395 and the haplotype "CCG" constructed by rs3918249, rs3918254 and rs3787268 were associated with increased risk of BC (P < 0.05). 30194384

2018

dbSNP: rs3918254
rs3918254
0.010 GeneticVariation BEFREE Additionally, the haplotype "AGTCA" constructed by rs3740938, rs2012390, rs1940475, rs11225394, and rs11225395 and the haplotype "CCG" constructed by rs3918249, rs3918254 and rs3787268 were associated with increased risk of BC (P < 0.05). 30194384

2018

dbSNP: rs17576
rs17576
0.010 GeneticVariation BEFREE No significant association was found between breast cancer risk and rs17576, rs2250889, and rs3787268 under any genetic models. 25890491

2015

dbSNP: rs17577
rs17577
0.010 GeneticVariation BEFREE In Stage 1, rare allele homozygotes for a promoter SNP (rs3918241) or a non-synonymous SNP (rs2274756, R668Q) tended to occur more frequently among breast cancer cases (P value = 0.116 and 0.056, respectively). 20725776

2011

dbSNP: rs2274756
rs2274756
0.010 GeneticVariation BEFREE In Stage 1, rare allele homozygotes for a promoter SNP (rs3918241) or a non-synonymous SNP (rs2274756, R668Q) tended to occur more frequently among breast cancer cases (P value = 0.116 and 0.056, respectively). 20725776

2011

dbSNP: rs3918241
rs3918241
0.010 GeneticVariation BEFREE In Stage 1, rare allele homozygotes for a promoter SNP (rs3918241) or a non-synonymous SNP (rs2274756, R668Q) tended to occur more frequently among breast cancer cases (P value = 0.116 and 0.056, respectively). 20725776

2011