ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.1328+37_1328+40del

dbSNP: rs145313346
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001523594 SCV001733323 benign not provided 2023-12-18 criteria provided, single submitter clinical testing
GeneDx RCV001523594 SCV001899563 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446804 SCV004172207 benign Retinitis pigmentosa 39 2023-04-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003446803 SCV004172208 benign Usher syndrome type 2A 2023-04-11 criteria provided, single submitter clinical testing

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