Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome.

Nevertheless, the less common SNP, rs2287839, which is located at the URR of this locus , showed a trend towards association with SPGF under the additive model that did not pass the FDR correction ( p addadj = 0.055, OR add = 1.38 (1.06–1.81)) ( Table 1 ).

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