A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci.

BMC Cancer · 2018 · PMC6310952 · PMID 30594178

Europe PMC DOI

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highly significantp = 1.2 × 10 − 23actually significant

Both variants were associated with expression levels of NBR2, CTD-3199 J23.6 and LINC00854 genes with a highly significant eQTL evidence for NBR2, a BRCA1 neighbor gene ( p = 1.2 × 10 − 23 and p = 2.1 × 10 − 25 for rs9911630 and rs799916, respectively) (Additional file 2 : Figure S1).

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