ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.3317-25dup

dbSNP: rs376363548
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001538095 SCV001755702 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001538095 SCV002458268 benign not provided 2023-08-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446814 SCV004172164 benign Retinitis pigmentosa 39 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446813 SCV004172165 benign Usher syndrome type 2A 2023-04-11 criteria provided, single submitter clinical testing

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