ClinVar Miner

Submissions for variant NM_001122681.2(SH3BP2):c.518-16C>A

dbSNP: rs367809628
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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 RCV002109759 SCV002393463 likely benign Fibrous dysplasia of jaw 2023-11-23 criteria provided, single submitter clinical testing

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