ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.1602G>A (p.Gly534=)

dbSNP: rs1266552493
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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 RCV001435579 SCV001638405 likely benign Cohen syndrome 2023-03-24 criteria provided, single submitter clinical testing

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