ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1366-6C>T

dbSNP: rs1564712471
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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 RCV002147099 SCV002413135 likely benign Gorlin syndrome; Medulloblastoma 2023-01-17 criteria provided, single submitter clinical testing

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