ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.10388-17_10388-7del

dbSNP: rs1442627890
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000731889 SCV000859757 uncertain significance not provided 2018-02-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000731889 SCV001706296 likely benign not provided 2023-11-09 criteria provided, single submitter clinical testing

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