ClinVar Miner

Submissions for variant NM_017617.5(NOTCH1):c.4128C>G (p.Gly1376=)

dbSNP: rs1292953898
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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 RCV001395894 SCV001597612 likely benign Adams-Oliver syndrome 5 2019-02-08 criteria provided, single submitter clinical testing

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