ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.7942-13T>G

gnomAD frequency: 0.00002  dbSNP: rs761317351
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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 RCV001395570 SCV001597284 likely benign Cohen syndrome 2023-06-27 criteria provided, single submitter clinical testing

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