Optimized high-throughput screening of non-coding variants identified from genome-wide association studies.

Nucleic Acids Res · 2023 · PMC9943666 · PMID 36546757

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nominally significantno p-value reported

Of these a total of 31 (39%) nominally significant SNPs passed multiple hypothesis testing correction (FDR < 0.05) with 23 being PCa disease-associated SNPs identified from GWAS.

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