Application of the STAAR framework in detecting rare variant associations with Alzheimer disease and related dementias: Insights and implications.

HGG Adv · 2026 · PMC12934298 · PMID 41560352

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highly significantno p-value reported

Further investigation revealed that only one of the SNPs (rs374374337) was highly significant in the single-variant analysis ( Table S3 ), with only a single alternative allele carrier.

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