Barely Significant
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The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians.

Nat Commun · 2022 · PMC9636136 · PMID 36333282

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marginally significantno p-value reported
The coding rs1047781 variant has been reported to display a marginally significant association with an indicator of liver damage (AST/ALT ratio), but the association with absolute levels of AST or ALT is novel 39 .

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