Rare heterozygous missense variants in VSX2 are associated with retinal detachment.

PLoS Genet · 2026 · PMC12890223 · PMID 41632798

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closest p · 1.0× alpha

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nominally significantp < 0.05actually significant

Extending this observation, we found a significant enrichment for other known recessive Mendelian eye disease genes among nominally significant (p < 0.05) genes associated with RD in the collapsing analysis.

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