Barely Significant
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Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

Sci Rep · 2016 · PMC5013272 · PMID 27600471

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borderline significantno p-value reported
In support of COX11 and TOM1L1 being the targets of this breast cancer susceptibility locus, eQTL analyses in normal breast tissue showed borderline significant associations of the risk alleles of top candidate causal SNP rs2787486 with increased expression levels of both TOM1L1 and COX11 ; candidate SNP rs2787481 also showed evidence of allelic imbalance in COX11 expression.

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