Identification of copy number variants contributing to hallux valgus.

Front Genet · 2023 · PMC10076598 · PMID 37035746

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marginal significanceno p-value reported

Genome-wide association study in population of European ancestry found the sex-specific association of SNVs close to genes AXIN2, ESD, ANXA1 and MRGPRX3 at the marginal significance level ( Hsu et al., 2015 ).

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