ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.708T>C (p.Thr236=)

dbSNP: rs2135872255
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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 RCV001443709 SCV001646693 likely benign Gorlin syndrome; Medulloblastoma 2019-06-14 criteria provided, single submitter clinical testing

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