Barely Significant
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Association between genetic risk variants and glucose intolerance during pregnancy in north Indian women.

BMC Med Genomics · 2018 · PMC6083526 · PMID 30089489

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nominally significantno p-value reported
For SNP rs5219 in KCNJ11 (HWE p = 0.004, WHO1999; HWE p = 0.01, WHO2013) and rs11605924 in CRY2 (HWE p = 0.007 WHO1999 and HWE p = 0.06, WHO2013), HWE values were nominally significant for the same criteria where an association was observed; these findings need to be replicated in independent cohorts.

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a trend towards significanceno p-value reported
Of 6 loci previously associated with insulin resistance, here 3 also showed an association with HOMA2-IR and a trend towards significance for GDM2013 but not GDM1999 including SNPs rs7607980 in the COBLL1 gene [ 40 ], rs13389219 near GRB14 and rs10423928 in the GIPR gene indicating that some of the genetic basis seem to be driven by previously reported insulin resistance loci.

also in 2,760 other papers

showed a trendno p-value reported
SNPs rs7607980 near COBLL1 ( p = 0.0001), rs13389219 near GRB14 ( p = 0.026) and rs10423928 in the GIPR gene ( p = 0.012) as well as the genetic risk score (GRS) for these previously shown insulin resistance loci here associated with insulin resistance defined by HOMA2-IR and showed a trend towards GDM.

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