Barely Significant
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Rare complement factor I variants associated with reduced macular thickness and age-related macular degeneration in the UK Biobank.

Hum Mol Genet · 2022 · PMC9402241 · PMID 35285476

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highly significantno p-value reported
In addition, we found highly significant interactions between CFH p.Y402H and ARMS2 p.A69S on AMD risk when either genotype existed in the homozygous state ( Table 6 ).

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