ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1023-8C>T

dbSNP: rs1554854552
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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 RCV000525343 SCV000623096 likely benign Gorlin syndrome; Medulloblastoma 2017-03-09 criteria provided, single submitter clinical testing

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