Genome-wide association study identifies multiple risk loci for renal cell carcinoma

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Abstract

Previous genome-wide association studies (GWAS) have identified six risk loci for renal cell carcinoma (RCC). We conducted a meta-analysis of two new scans of 5,198 cases and 7,331 controls together with four existing scans, totalling 10,784 cases and 20,406 controls of European ancestry. Twenty-four loci were tested in an additional 3,182 cases and 6,301 controls. We confirm the six known RCC risk loci and identify seven new loci at 1p32.3 (rs4381241, P = 3.1×10-10), 3p22.1 (rs67311347, P = 2.5×10-8), 3q26.2 (rs10936602, P = 8.8×10-9), 8p21.3 (rs2241261, P = 5.8×10-9), 10q24.33-q25.1 (rs11813268, P = 3.9×10-8), 11q22.3 (rs74911261, P = 2.1×10-10) and 14q24.2 (rs4903064, P = 2.2×10-24). Expression quantitative trait analyses suggest plausible candidate genes at these regions that may contribute to RCC susceptibility.

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Scelo, G., Purdue, M. P., Brown, K. M., Johansson, M., Wang, Z., Eckel-Passow, J. E., … Chanock, S. J. (2017). Genome-wide association study identifies multiple risk loci for renal cell carcinoma. Nature Communications, 8. https://doi.org/10.1038/ncomms15724

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