ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1158-15T>C

dbSNP: rs998644443
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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 RCV002204484 SCV002494239 likely benign Gorlin syndrome; Medulloblastoma 2023-12-16 criteria provided, single submitter clinical testing

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