Barely Significant
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Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia.

Transl Psychiatry · 2018 · PMC6251918 · PMID 30470734

1
hedged sentence
0.0000
closest p · 0.0× alpha
0.0000
boldest claim

The sentences

nominally significantp = 5.14 × 10 −7actually significant
The first of these regions is located on chromosome 2 and includes nominally significant SCZ variant (top variant in PGC: rs10189857, p = 5.14 × 10 −7 ) 19 in an intron of BCL11A , and a T2D risk locus upstream of the same gene (top variant in DIAGRAMv3: rs243021, p = 3 × 10 −15 ) 46 .

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