ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.2331G>A (p.Pro777=)

gnomAD frequency: 0.00001  dbSNP: rs1445735832
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000924872 SCV001070398 likely benign not provided 2018-08-09 criteria provided, single submitter clinical testing

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