ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.4075-6C>T (rs377411812)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000711533 SCV000841911 benign not provided 2018-03-08 criteria provided, single submitter clinical testing
GeneDx RCV000435109 SCV000524600 likely benign not specified 2016-03-02 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

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