ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1296+9G>T

gnomAD frequency: 0.00001  dbSNP: rs759664715
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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 RCV001489281 SCV001693820 likely benign Gorlin syndrome; Medulloblastoma 2022-05-18 criteria provided, single submitter clinical testing

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