Barely Significant
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NTHL1 is a recessive cancer susceptibility gene.

Sci Rep · 2023 · PMC10689455 · PMID 38036545

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nominally significantP < 0.05actually significant
We detected two variants, MAD1L1 NM_001013836.2 :c.1947C>G p.(Tyr649Ter) and USP45 NM_001346022.3 :c.2190C>A p.(Tyr730Ter), with a higher frequency in the patients than in the controls on a nominally significant level (P < 0.05) (Table 1 ); however, another pLoF in the USP45 gene, NM_001346022.3 :c.1008del p.(Val337SerfsTer9), was found only slightly more often in the patients than in the controls.

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