Barely Significant
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Elucidating clinical phenotypic variability associated with the polyT tract and TG repeats in CFTR.

Hum Mutat · 2021 · PMC9292755 · PMID 34196078

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showed a trendno p-value reported
Unfortunately, the small number of individuals in the population with a TG13T5 variant limited the number of homozygous individuals available for assessment, although these individuals showed a trend in enrichment similar to patients with CFvar/CFvar genotypes.

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