Barely Significant
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Unmet Needs in Systemic Sclerosis Understanding and Treatment: the Knowledge Gaps from a Scientist's, Clinician's, and Patient's Perspective.

Clin Rev Allergy Immunol · 2018 · PMC6244948 · PMID 28866756

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highly significantno p-value reported
have elegantly shown that only 20% of the estimated SSc heritability is to date documented in terms of highly significant and robustly replicated single nucleotide polymorphisms (SNPs) associations [ 30 ].

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