Significant Association of rs2147555 Genetic Polymorphism in the <i>EDNRB</i> Gene with Hirschsprung Disease in Southern Chinese Children.

Biomed Res Int · 2020 · PMC7648675 · PMID 33178831

Europe PMC DOI

hedged sentences

—

closest p

—

boldest claim

The sentences

highly significantno p-value reported

In conclusion, the C allele of SNP rs2147555 of EDNRB on chromosome 13q22 confers a highly significant risk of HSCR in the Southern Chinese population.

also in 132,142 other papers

marginally significantno p-value reported

We found marginally significant allelic C association with L-HSCR, and genotypic and recessive models also showed significant associations (Tables 2 and 3 ).

also in 26,082 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.