ClinVar Miner

Submissions for variant NM_025152.3(NUBPL):c.693+98A>G

gnomAD frequency: 0.95998  dbSNP: rs1540425
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 RCV001718563 SCV001945110 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001718563 SCV005291191 benign not provided criteria provided, single submitter not provided

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