ClinVar Miner

Submissions for variant NM_033305.3(VPS13A):c.3508-8T>C

gnomAD frequency: 0.00031  dbSNP: rs376751858
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000863503 SCV001004177 likely benign not provided 2024-11-11 criteria provided, single submitter clinical testing
Natera, Inc. RCV001276368 SCV001462580 likely benign Chorea-acanthocytosis 2020-09-16 no assertion criteria provided clinical testing

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