Excess of rare noncoding variants in several type 2 diabetes candidate genes among Asian Indian families.

Commun Med (Lond) · 2025 · PMC11846969 · PMID 39987249

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marginally significantno p-value reported

At the same time, a marginally significant burden on T2D was observed in CMC T 2 and CMC regression analysis in the new gene SLC38A11 (Table 2 ).

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