Clinical Study

Association between Functional Polymorphisms of Foxp3 Gene and the Occurrence of Unexplained Recurrent Spontaneous Abortion in a Chinese Han Population

Figure 2

Schematic structure of the human Foxp3 gene and the linkage disequilibrium as determined in the URSA population (Haploview 4.20 version). The coding sequences, noncoding sequences and the introns were depicted as black boxes, white boxes, and horizontal lines, respectively. Exon numbers were shown below the exon boxes. The sizes of exons and introns were labeled above them. The locations of rs5902434 (1), rs3761548 (2), rs2232365 (3), rs2294021 (4), (GT)n microsatellite polymorphisms, the start cordon, and the stop cordon were indicated by arrows. The standard (D/LOD) was represented by red color and r 2 was presented as a number if it deviates from 100.
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