ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.3225T>C (p.Ser1075=)

dbSNP: rs2133440516
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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 RCV002206487 SCV002494063 likely benign Cohen syndrome 2023-11-24 criteria provided, single submitter clinical testing

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