ClinVar Miner

Submissions for variant NM_033305.3(VPS13A):c.144+15T>C

gnomAD frequency: 0.00029  dbSNP: rs182861770
Minimum review status: Collection method:
Minimum conflict level:
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 RCV002213411 SCV002367790 benign not provided 2024-12-26 criteria provided, single submitter clinical testing

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