ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.489+42C>T

gnomAD frequency: 0.07042  dbSNP: rs41289315
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 RCV001685751 SCV001897362 benign not provided 2019-06-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001685751 SCV005317003 benign not provided criteria provided, single submitter not provided

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