ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.683+7A>G

dbSNP: rs764695403
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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 RCV001473821 SCV001677982 likely benign Gorlin syndrome; Medulloblastoma 2022-02-24 criteria provided, single submitter clinical testing

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