ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.5670C>T (p.Val1890=)

dbSNP: rs1588579765
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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 RCV001433709 SCV001636503 likely benign Cohen syndrome 2018-08-30 criteria provided, single submitter clinical testing

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