Barely Significant
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Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.

PLoS One · 2012 · PMC3302824 · PMID 22428046

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near-significantno p-value reported
In addition, the SNP-based linkage analysis identified a near-significant region of 0.19 Mb on Xp22.33, that spans the boundary between the pseudo-autosomal region and the X specific region (LOD = 2.94, figure 2 ).

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