Barely Significant
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Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families.

BMC Med Genet · 2019 · PMC6357511 · PMID 30704416

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highly significantno p-value reported
We did initially find a single SNP that was out of HWE at 16q22.1 that had a highly significant for two-point logarithm of the odds (LOD) score of 7.76.

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