ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1185T>C (p.Phe395=)

dbSNP: rs760982248
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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 RCV002161690 SCV002477143 likely benign Gorlin syndrome; Medulloblastoma 2023-05-15 criteria provided, single submitter clinical testing

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