ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1365+13G>C

gnomAD frequency: 0.00001  dbSNP: rs1370046167
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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 RCV002192802 SCV002360118 likely benign Gorlin syndrome; Medulloblastoma 2021-08-02 criteria provided, single submitter clinical testing

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