ClinVar Miner

Submissions for variant NM_001805.4(CEBPE):c.18C>T (p.Tyr6=)

dbSNP: rs776516349
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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 RCV001421460 SCV001623984 likely benign Specific granule deficiency 2020-08-22 criteria provided, single submitter clinical testing

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