ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1077G>A (p.Glu359=)

dbSNP: rs1590082194
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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 RCV001403350 SCV001605219 likely benign Gorlin syndrome; Medulloblastoma 2018-09-17 criteria provided, single submitter clinical testing

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