ClinVar Miner

Submissions for variant NM_017617.5(NOTCH1):c.1848C>A (p.Gly616=)

dbSNP: rs776185489
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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 RCV003748680 SCV004512654 likely benign Adams-Oliver syndrome 5 2023-09-17 criteria provided, single submitter clinical testing

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