ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.183-17T>C

gnomAD frequency: 0.00004  dbSNP: rs767300975
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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 RCV002200633 SCV002488722 likely benign Gorlin syndrome; Medulloblastoma 2023-12-29 criteria provided, single submitter clinical testing

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