ClinVar Miner

Submissions for variant NM_000500.9(CYP21A2):c.293-13C>T (rs6467)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centro de Desenvolvimento Científico e Tecnológico, Secretaria da Saúde do Estado do Rio Grande do Sul RCV000502480 SCV000580686 not provided Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency no assertion provided research

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