ClinVar Miner

Submissions for variant NM_001122681.2(SH3BP2):c.358-13C>T

gnomAD frequency: 0.00001  dbSNP: rs199799999
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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 RCV002109998 SCV002439972 likely benign Fibrous dysplasia of jaw 2023-08-04 criteria provided, single submitter clinical testing

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