ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1023-18C>A

gnomAD frequency: 0.00001  dbSNP: rs892399500
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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 RCV002154251 SCV002461735 likely benign Gorlin syndrome; Medulloblastoma 2022-02-10 criteria provided, single submitter clinical testing

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