Barely Significant
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UGT2B17 copy number gain in a large ankylosing spondylitis multiplex family.

BMC Genet · 2013 · PMC3751806 · PMID 23927372

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only marginally significantno p-value reported
However, two copies of the UGT2B17 gene CNV were only marginally significant in a uniplex AS cohort from Newfoundland but not in a uniplex AS cohort from Alberta.

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