In silico prioritisation of microRNA-associated common variants in multiple sclerosis.

Hum Genomics · 2023 · PMC10061723 · PMID 36991503

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nominally significantno p-value reported

Nominally significant SNPs which did not meet the genome-wide threshold were extracted from the IMSGC [ 6 ] Additional files (Additional file 1 : Table S14).

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