ClinVar Miner

Submissions for variant NM_005618.4(DLL1):c.1650C>T (p.Ala550=)

gnomAD frequency: 0.00207  dbSNP: rs146859652
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000900019 SCV001044316 benign not provided 2024-01-01 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000900019 SCV004158652 likely benign not provided 2024-03-01 criteria provided, single submitter clinical testing DLL1: BP4, BP7

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