ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.6351C>T (p.Ser2117=)

dbSNP: rs1599359717
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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 RCV000929401 SCV001075031 likely benign not provided 2018-09-19 criteria provided, single submitter clinical testing

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