ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1158-8_1158-7insCTG

dbSNP: rs2135934830
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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 RCV001506181 SCV001711098 likely benign Gorlin syndrome; Medulloblastoma 2022-12-06 criteria provided, single submitter clinical testing

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