ClinVar Miner

Submissions for variant NM_199242.3(UNC13D):c.1878C>T (p.His626=)

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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 RCV002590414 SCV002958008 likely benign Familial hemophagocytic lymphohistiocytosis 3 2023-12-12 criteria provided, single submitter clinical testing

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