Barely Significant
← all excerpts

Association of Single Nucleotide Polymorphisms on Locus 18q21.1 in the Etiology of Nonsyndromic Cleft Lip Palate (NSCLP) in Indian Multiplex Families.

Glob Med Genet · 2021 · PMC7964250 · PMID 33748821

1
hedged sentence
closest p
boldest claim

The sentences

highly significantno p-value reported
Fine mapping of the locus 18q21.1 revealed rs183559995 of MYO5B showed highly significant association with an OR of 18.09.

also in 132,142 other papers

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.