The risks of RELN polymorphisms and its expression in the development of otosclerosis.

PLoS One · 2022 · PMC9165908 · PMID 35658052

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highly significantno p-value reported

A highly significant difference was observed for rs3914132 in the allele count of the cases 46/508 (0.09) and the controls 78/524 (0.15).

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showed a trendno p-value reported

Previously, we showed a trend towards association of this polymorphism with OTSC and identified a rare variant rs74503667 in a familial case.

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