ClinVar Miner

Submissions for variant NM_000096.4(CP):c.2879-1G>T (rs386134141)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Hemoglobin and Genome Lab,University of Campinas RCV000496109 SCV000586732 likely pathogenic Deficiency of ferroxidase 2017-07-28 criteria provided, single submitter research

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