ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.9332A>T (p.Tyr3111Phe)

dbSNP: rs199704158
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001677613 SCV001894633 benign not provided 2019-01-02 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003987896 SCV004804467 likely benign not specified 2024-01-11 criteria provided, single submitter clinical testing
Natera, Inc. RCV001836471 SCV002082710 benign Cohen syndrome 2019-08-26 no assertion criteria provided clinical testing

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