ClinVar Miner

Submissions for variant NM_019074.4(DLL4):c.659-77C>T

gnomAD frequency: 0.03386  dbSNP: rs7174607
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 RCV001677702 SCV001893714 benign not provided 2018-11-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001677702 SCV005296839 benign not provided criteria provided, single submitter not provided

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