ClinVar Miner

Submissions for variant NM_004946.3(DOCK2):c.6C>A (p.Ala2=)

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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 RCV002866592 SCV003234647 likely benign DOCK2 deficiency 2022-09-10 criteria provided, single submitter clinical testing

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