ClinVar Miner

Submissions for variant NM_001122681.2(SH3BP2):c.1662C>T (p.Pro554=)

dbSNP: rs775871629
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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 RCV002075955 SCV002428504 likely benign Fibrous dysplasia of jaw 2022-06-10 criteria provided, single submitter clinical testing

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