ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.996C>T (p.Arg332=)

gnomAD frequency: 0.00016  dbSNP: rs183500505
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
Athena Diagnostics RCV001288902 SCV001476308 benign not specified 2019-12-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002069557 SCV002404991 benign not provided 2023-11-24 criteria provided, single submitter clinical testing

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