ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.624C>T (p.Asn208=)

gnomAD frequency: 0.00009  dbSNP: rs368179321
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 RCV001663877 SCV001879636 likely benign not specified 2020-11-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003546711 SCV004265478 likely benign not provided 2022-12-03 criteria provided, single submitter clinical testing

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