ClinVar Miner

Submissions for variant NC_000010.11:g.(?_102593630)_(102597299_?)del

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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 RCV000628526 SCV000749428 pathogenic Gorlin syndrome; Medulloblastoma 2021-08-04 criteria provided, single submitter clinical testing

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