near-significantp = 0.035
However, the PCDH15 rs10763170 minor allele (T allele) presented a near-significant association with somatotrophinomas (dominant inheritance model, OR 1.55, 95% CI 1.02–2.35, p = 0.035).
However, the PCDH15 rs10763170 minor allele (T allele) presented a near-significant association with somatotrophinomas (dominant inheritance model, OR 1.55, 95% CI 1.02–2.35, p = 0.035).
The NEBL rs2359536 and PCDH15 rs10763170 variants were not associated with the overall risk for the disease, although a borderline significant association was observed between the PCDH15 rs10763170 minor allele (T allele) and somatotrophinomas (dominant model, OR 1.55, 95% CI 1.02–2.35, p = 0.035).
Although the association with these variants was highly significant in the Han Chinese population, these results have not yet been confirmed in any other population.