Barely Significant
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ANO2 Genetic Variants and Anti-VEGF Treatment Response in Neovascular AMD: A Pharmacogenetic Substudy of VIEW 1 and VIEW 2.

Invest Ophthalmol Vis Sci · 2024 · PMC11244643 · PMID 38980270

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closest p · 0.0× alpha
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The sentences

highly significantP = 1.99 × 10 –8actually significant
A cluster of variants in ANO2 (encoding anoctamin 2, a calcium-activated chloride channel expressed on photoreceptor cells) on chromosome 12 reached the level of significance for loss of ≥5 letters after 1 year of treatment ( P < 5 × 10 –8 ), with the ANO2 rs2110166 SNP demonstrating highly significant association ( P = 1.99 × 10 –8 ).

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