ClinVar Miner

Submissions for variant NM_020821.3(VPS13C):c.387C>T (p.Gly129=) (rs139665824)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000660525 SCV000782627 uncertain significance Parkinson disease 23, autosomal recessive early-onset 2017-04-12 criteria provided, single submitter clinical testing
Invitae RCV000913670 SCV001058824 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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