Barely Significant
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Genetic associations with neonatal thyroid-stimulating hormone levels.

Pediatr Res · 2013 · PMC3775497 · PMID 23344678

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only marginally significantno p-value reported
Although, only rs965513 meets multiple testing correction level of significance while the other two SNPs are only marginally significant, this may be secondary to the moderate, but not complete, linkage disequilibrium (LD) with each other (rs965513, rs1443432: D’=0.863, r-squared =0.519; rs965513, rs3021523: D’=0.835, r-squared=0.48) and where rs965513 and rs1443433 also have strong effects as part of a haplotype associated with TSH levels.

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