ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.10528+77T>C

gnomAD frequency: 0.00047  dbSNP: rs74787946
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 RCV001556580 SCV001778189 likely benign not provided 2019-05-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001556580 SCV005226958 likely benign not provided criteria provided, single submitter not provided

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