Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12484776
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

dbSNP: rs12484776
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

dbSNP: rs12484776
rs12484776
G 0.820 GeneticVariation GWASDB A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. 21460842

2011

dbSNP: rs12484776
rs12484776
G 0.820 GeneticVariation GWASCAT A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. 21460842

2011