ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.276T>A (p.Leu92=)

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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 RCV002810730 SCV003209582 likely benign Cohen syndrome 2022-05-30 criteria provided, single submitter clinical testing

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