ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.8064T>C (p.Ser2688=)

dbSNP: rs1456443971
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000931622 SCV001077292 likely benign not provided 2022-04-08 criteria provided, single submitter clinical testing
Natera, Inc. RCV001271974 SCV001453601 uncertain significance Usher syndrome type 2A 2020-03-10 no assertion criteria provided clinical testing

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