ClinVar Miner

Submissions for variant NM_004946.3(DOCK2):c.979+8G>A

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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 RCV003082625 SCV003483844 likely benign DOCK2 deficiency 2023-10-03 criteria provided, single submitter clinical testing

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