ClinVar Miner

Submissions for variant NM_015378.4(VPS13D):c.10260T>C (p.Phe3420=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003422594 SCV004128525 likely benign not provided 2022-07-01 criteria provided, single submitter clinical testing VPS13D: BP4

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