ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.4104+4A>T

dbSNP: rs483353052
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory; Baylor College of Medicine RCV000119816 SCV000154742 unknown Usher syndrome type 1D criteria provided, single submitter not provided Converted during submission to Uncertain significance.

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