ClinVar Miner

Submissions for variant NM_000441.2(SLC26A4):c.1668T>A (p.Tyr556Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Indian Institute of Integrative Medicine,Council of Scientific and Industrial Research RCV001269338 SCV001448681 likely pathogenic SLC26A4-Related Disorders 2020-02-15 no assertion criteria provided research Carriers (Heterozygous) were found in this study.

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