ClinVar Miner

Submissions for variant NM_001122681.2(SH3BP2):c.1008C>T (p.Ser336=)

dbSNP: rs1724887772
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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 RCV001454357 SCV001658080 likely benign Fibrous dysplasia of jaw 2024-10-16 criteria provided, single submitter clinical testing

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