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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |