ClinVar Miner

Submissions for variant NM_016030.6(TRAPPC12):c.1777-15A>C

gnomAD frequency: 0.01406  dbSNP: rs73910562
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 RCV002118107 SCV002404993 benign not provided 2025-01-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002118107 SCV005283804 benign not provided criteria provided, single submitter not provided

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