ClinVar Miner

Submissions for variant NM_022356.4(P3H1):c.618+10dup

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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 RCV003601417 SCV004399869 benign Osteogenesis imperfecta type 8 2023-06-28 criteria provided, single submitter clinical testing

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