ClinVar Miner

Submissions for variant NM_019074.4(DLL4):c.336+17C>T

gnomAD frequency: 0.00118  dbSNP: rs369890870
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002113998 SCV002438304 benign not provided 2024-12-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002113998 SCV005296834 benign not provided criteria provided, single submitter not provided

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