ClinVar Miner

Submissions for variant NM_001122681.2(SH3BP2):c.240-14C>T

gnomAD frequency: 0.00004  dbSNP: rs763517516
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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 RCV002102563 SCV002387678 likely benign Fibrous dysplasia of jaw 2023-10-12 criteria provided, single submitter clinical testing

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