ClinVar Miner

Submissions for variant NM_001039591.3(USP9X):c.4603+19A>G

gnomAD frequency: 0.00771  dbSNP: rs55900117
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514923 SCV000610091 likely benign not provided 2017-04-12 criteria provided, single submitter clinical testing
GeneDx RCV000514923 SCV001825423 likely benign not provided 2018-09-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000514923 SCV002494152 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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