ClinVar Miner

Submissions for variant NM_001830.4(CLCN4):c.287C>T (p.Thr96Met)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003563693 SCV004312660 benign not provided 2023-07-25 criteria provided, single submitter clinical testing

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