The landscape of rare genetic variants in familial Waldenström macroglobulinemia.

Blood Neoplasia · 2024 · PMC11258892 · PMID 39036705

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nearly significantno p-value reported

A single SNV (rs9838238) in DCBLD2 (discoidin, CUB and LCCL domain containing 2) was nearly significant after Bonferroni correction.

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