ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.455-19C>A

dbSNP: rs370818590
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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 RCV002146581 SCV002462898 likely benign Gorlin syndrome; Medulloblastoma 2024-01-28 criteria provided, single submitter clinical testing

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