ClinVar Miner

Submissions for variant NM_199242.3(UNC13D):c.388+15G>C

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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 RCV003498973 SCV004261579 likely benign Familial hemophagocytic lymphohistiocytosis 3 2024-01-17 criteria provided, single submitter clinical testing

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