The First Report of a Missense Variant in <i>RFX2</i> Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani Family.

Front Genet · 2021 · PMC8822170 · PMID 35145545

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highly significantno p-value reported

Moreover, the RFX2 variant achieved highly significant CADD (27.3) and GERP (5.1399) scores ( Table 2 ).

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