ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.5323G>A (p.Ala1775Thr)

gnomAD frequency: 0.00009  dbSNP: rs139983430
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002023584 SCV002304664 benign not provided 2022-09-07 criteria provided, single submitter clinical testing

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