ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1366-18T>C

gnomAD frequency: 0.00001  dbSNP: rs778922691
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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 RCV002112701 SCV002392980 likely benign Gorlin syndrome; Medulloblastoma 2023-12-11 criteria provided, single submitter clinical testing

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