ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.598-4T>C

dbSNP: rs2135870306
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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 RCV001500348 SCV001705133 likely benign Gorlin syndrome; Medulloblastoma 2019-12-03 criteria provided, single submitter clinical testing

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