ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.597+11G>A

dbSNP: rs754485815
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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 RCV002119673 SCV002396477 likely benign Gorlin syndrome; Medulloblastoma 2021-08-03 criteria provided, single submitter clinical testing

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