ClinVar Miner

Submissions for variant NM_001122681.2(SH3BP2):c.1482G>A (p.Ser494=)

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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 RCV003878514 SCV004677987 likely benign Fibrous dysplasia of jaw 2023-05-11 criteria provided, single submitter clinical testing

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