ClinVar Miner

Submissions for variant NM_000441.2(SLC26A4):c.1572C>T (p.Ile524=) (rs1562837305)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000730419 SCV000858153 uncertain significance not provided 2017-11-28 criteria provided, single submitter clinical testing

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