ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.6463-24T>G

gnomAD frequency: 0.00775  dbSNP: rs75312629
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001545257 SCV001764555 likely benign not provided 2019-02-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001545257 SCV005226985 likely benign not provided criteria provided, single submitter not provided

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