|
rs7958904
|
|
|
0.060 |
GeneticVariation |
BEFREE |
For the rs7958904 polymorphism, we obtained the polymorphism significantly decreased susceptibility to overall cancer risk among five genetic models rather than recessive and homozygous models.
|
29463216 |
2018 |
|
rs7958904
|
|
|
0.060 |
GeneticVariation |
BEFREE |
The results showed that cancer risk was elevated in recessive mutation of rs12826786 (TT vs CC+CT: OR =1.55, 95% CI =1.19, 2.03; TT+CT vs CC: OR =1.23, 95% CI =1.04, 1.46; TT vs CC: OR =1.67, 95% CI =1.24, 2.24; T vs C: OR =1.24, 95% CI =1.09, 1.40) and rs920778 (TT vs CC+CT: OR =1.73, 95% CI =1.30, 2.30; TT+CT vs CC: OR =1.40, 95% CI =1.16, 1.70; TT vs CC: OR =1.83, 95% CI =1.25, 2.68; T vs C: OR =1.37, 95% CI =1.18, 1.59), while the results for polymorphisms of rs7958904, rs4759314, rs874945, and rs1899663 were insignificant.
|
29497311 |
2018 |
|
rs7958904
|
|
|
0.060 |
GeneticVariation |
BEFREE |
HOTAIR SNP rs920778, rs7958904 and rs874945 are susceptible to cancer risk.
|
27965458 |
2017 |
|
rs7958904
|
|
|
0.060 |
GeneticVariation |
BEFREE |
For the rs7958904 polymorphism we detected a significantly decreased susceptibility to overall cancer in all 5 genetic models rather than the heterogeneous model.
|
27791260 |
2017 |
|
rs7958904
|
|
|
0.060 |
GeneticVariation |
BEFREE |
However, significant decreases in cancer risk were observed for rs7958904 in the total population, as well as in subgroup analyses.
|
28938673 |
2017 |
|
rs7958904
|
|
|
0.060 |
GeneticVariation |
BEFREE |
The results also suggested that other SNPs were correlated with overall cancer risk, namely, two in HOTAIR (HOX transcript antisense RNA: rs920778C/T and rs7958904 G/C) and two in PRNCR1 (rs1016343C/T and rs16901946 A/G).
|
28342449 |
2017 |