ClinVar Miner

Submissions for variant NM_018206.6(VPS35):c.1893C>T (p.Ile631=)

gnomAD frequency: 0.00002  dbSNP: rs1183192271
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001497615 SCV001702350 likely benign Parkinson disease 17 2020-03-03 criteria provided, single submitter clinical testing

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