We observed a non-significant association of histology with age at diagnosis (>65 versus ≤60), grade, microsatellite instability (MSI) status, lymphatic invasion (LI), and BRAF V600E mutation; a moderately significant association with stage, sex, and age at diagnosis between 60 and 65 versus ≤60; and a strongly significant association with tumor location (Table 1 ).
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Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses.
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