ClinVar Miner

Submissions for variant NM_033305.3(VPS13A):c.4631-17A>G

gnomAD frequency: 0.00079  dbSNP: rs188844161
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 RCV002213127 SCV002364862 benign not provided 2025-01-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002213127 SCV005268594 benign not provided criteria provided, single submitter not provided

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