ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.4633+22dup

dbSNP: rs756149542
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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 RCV002141120 SCV002467403 benign Cohen syndrome 2024-01-24 criteria provided, single submitter clinical testing

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