ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.597+8A>C

dbSNP: rs2135867474
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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 RCV001417820 SCV001620026 likely benign Gorlin syndrome; Medulloblastoma 2020-10-15 criteria provided, single submitter clinical testing

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