ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.413-5T>C

dbSNP: rs1846839473
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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 RCV001470280 SCV001674375 likely benign Cohen syndrome 2023-09-08 criteria provided, single submitter clinical testing

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