Interpretation of genomic variants using a unified biological network approach.

PLoS Comput Biol · 2013 · PMC3591262 · PMID 23505346

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highly significantno p-value reported

For example, a moderately deleterious missense SNV in a highly significant gene can be equally or more damaging than a strongly deleterious missense SNV in a less significant gene.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.