|
rs2280543
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Two SNPs, rs2280543 from BET1L (χ<sup>2</sup> = 18.3, OR = 0.64, P = 1.87 × 10<sup>-5</sup>) and rs12484776 from TNRC6B (χ<sup>2</sup> = 19.7, OR = 1.40, P = 8.91 × 10<sup>-6</sup>), were identified as significantly associated with the disease status of UL.
|
29743541 |
2018 |
|
rs2280543
|
|
|
0.830 |
GeneticVariation |
BEFREE |
The rs12484776 significantly contributes to UL risk among Saudi women, both in single and also in synergistic cooperation with rs2280543, rs7913069, and rs1056836 markers.
|
27987337 |
2017 |
|
rs2280543
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Meta-analysis showed a strong association at blocked early in transport 1 homolog (BET1L) rs2280543 for intramural UFs (meta-OR = 0.51, standard error (SE) = 0.14, Q = 0.590, I = 0, p = 2.48 × 10(-6)), which is stronger than the overall association with UF risk.
|
23892540 |
2013 |
|
rs2280543
|
|
G |
0.830 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
rs2280543
|
|
G |
0.830 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
rs12484776
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Two SNPs, rs2280543 from BET1L (χ<sup>2</sup> = 18.3, OR = 0.64, P = 1.87 × 10<sup>-5</sup>) and rs12484776 from TNRC6B (χ<sup>2</sup> = 19.7, OR = 1.40, P = 8.91 × 10<sup>-6</sup>), were identified as significantly associated with the disease status of UL.
|
29743541 |
2018 |
|
rs12484776
|
|
|
0.820 |
GeneticVariation |
BEFREE |
The rs12484776 significantly contributes to UL risk among Saudi women, both in single and also in synergistic cooperation with rs2280543, rs7913069, and rs1056836 markers.
|
27987337 |
2017 |
|
rs12484776
|
|
G |
0.820 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
rs12484776
|
|
G |
0.820 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
rs7913069
|
|
|
0.810 |
GeneticVariation |
BEFREE |
The rs12484776 significantly contributes to UL risk among Saudi women, both in single and also in synergistic cooperation with rs2280543, rs7913069, and rs1056836 markers.
|
27987337 |
2017 |
|
rs7913069
|
|
A |
0.810 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
rs7913069
|
|
A |
0.810 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
|
21460842 |
2011 |
|
rs4247357
|
|
|
0.710 |
GeneticVariation |
BEFREE |
Direct sequencing of this genomic region might be warranted to determine whether rs4247357, or some other variant, is causally related to UL.
|
27375065 |
2016 |
|
rs4247357
|
|
|
0.710 |
GeneticVariation |
GWASDB |
Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata.
|
23040493 |
2012 |
|
rs10508765
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |
|
rs10815466
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |
|
rs10835889
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.
|
31249589 |
2019 |
|
rs10917151
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.
|
31249589 |
2019 |
|
rs10976689
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |
|
rs11031006
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |
|
rs11178393
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |
|
rs11246003
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |
|
rs116251328
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |
|
rs117245733
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |
|
rs12224688
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
|
31649266 |
2019 |