ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.7671T>C (p.Asp2557=)

dbSNP: rs1414554416
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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 RCV002199628 SCV002352034 likely benign Cohen syndrome 2022-06-17 criteria provided, single submitter clinical testing

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