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A. Semenova

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Open access Aug 2026

CHEK2 Germline Variants in Cancer Predisposition: Whole Genome Sequencing Results

Assessment of the role of germline CHEK2 variants in the development of different cancer types confirmed that CHEK2 c.470T>C is the most common variant in the patient group, and the contribution of this variant to hereditary cancer risk in the Russian population is modest.

M. Nemtsova, M. Makarova, Anastasiia M. Danishevich et al. · 0 citations

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