ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.5733+37G>A

dbSNP: rs3817218
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 RCV001689332 SCV001914977 benign not provided 2018-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001689332 SCV005316944 benign not provided criteria provided, single submitter not provided

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