ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.10740+7G>A

dbSNP: rs201206110
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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 RCV000944662 SCV001090639 likely benign not provided 2023-12-26 criteria provided, single submitter clinical testing
Natera, Inc. RCV001274949 SCV001459533 uncertain significance Usher syndrome type 2A 2019-12-27 no assertion criteria provided clinical testing

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