ClinVar Miner

Submissions for variant NM_033305.3(VPS13A):c.4114+52C>T

gnomAD frequency: 0.01657  dbSNP: rs78364594
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
GeneDx RCV001677586 SCV001894598 benign not provided 2018-07-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001677586 SCV005268591 benign not provided criteria provided, single submitter not provided

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