Barely Significant
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Genomic landscape of patients with germline RUNX1 variants and familial platelet disorder with myeloid malignancy.

Blood Adv · 2024 · PMC10837196 · PMID 38019014

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may not be significantno p-value reported
LRP1B is a large (90 exons) gene, so the detected LRP1B mutations may not be significant.

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