ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.6024G>A (p.Pro2008=)

gnomAD frequency: 0.00007  dbSNP: rs766274305
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 RCV000954170 SCV001100784 likely benign not provided 2025-01-06 criteria provided, single submitter clinical testing
Athena Diagnostics RCV001288541 SCV001475720 benign not specified 2019-12-03 criteria provided, single submitter clinical testing

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