ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.987T>G (p.Pro329=)

dbSNP: rs906267027
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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 RCV002182754 SCV002349922 likely benign Gorlin syndrome; Medulloblastoma 2021-10-12 criteria provided, single submitter clinical testing

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