ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.78C>T (p.Phe26=)

dbSNP: rs2135597954
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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 RCV002198690 SCV002484507 likely benign Gorlin syndrome; Medulloblastoma 2023-12-06 criteria provided, single submitter clinical testing

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