ClinVar Miner

Submissions for variant NM_001144967.3(NEDD4L):c.1980T>C (p.Tyr660=)

gnomAD frequency: 0.00075  dbSNP: rs202013710
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000473115 SCV000563285 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
GeneDx RCV000473115 SCV001898707 benign not provided 2021-01-07 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000473115 SCV004143180 likely benign not provided 2023-02-01 criteria provided, single submitter clinical testing NEDD4L: BP4, BP7

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