ClinVar Miner

Submissions for variant NM_017617.5(NOTCH1):c.1644C>T (p.Asn548=)

gnomAD frequency: 0.00001  dbSNP: rs776488663
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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 RCV001398806 SCV001600581 likely benign Adams-Oliver syndrome 5 2019-11-30 criteria provided, single submitter clinical testing

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