ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.933C>T (p.Thr311=)

dbSNP: rs767071744
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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 RCV002093783 SCV002429942 likely benign Gorlin syndrome; Medulloblastoma 2020-11-30 criteria provided, single submitter clinical testing

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