Barely Significant
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Hereditable variants of classical protein tyrosine phosphatase genes: Will they prove innocent or guilty?

Front Cell Dev Biol · 2022 · PMC9900141 · PMID 36755664

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marginal significanceno p-value reported
Furthermore, a type 2 diabetes-related CNV (nsv8414) with marginal significance was detected for PTPRD ( Yan et al., 2018 ) and intronic SNP rs17584,499 in the gene significantly associated ( p = 8.5×10 −10 ) with the incidence of this disease in the Chinese population ( Tsai et al., 2010 ; Chen et al., 2021b ).

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