Clinical Relevance of +936 C>T <i>VEGFA</i> and c.233C>T <i>bFGF</i> Polymorphisms in Chronic Lymphocytic Leukemia.

Genes (Basel) · 2020 · PMC7349122 · PMID 32585853

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did not reach statistical significanceno p-value reported

Although the rs1449683 bFGF SNP did not reach statistical significance as a B-CLL predisposition factor, this SNP associated significantly with high genetic risk (a very relevant marker of B-CLL disease progression) in patients.

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