ClinVar Miner

Submissions for variant NM_019074.4(DLL4):c.1021-46C>T

gnomAD frequency: 0.07122  dbSNP: rs2277538
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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 RCV001615798 SCV001836814 benign not provided 2018-12-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615798 SCV005296841 benign not provided criteria provided, single submitter not provided

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