ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.14595A>G (p.Gln4865=)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002286174 SCV002576073 likely benign not provided 2020-07-20 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Labcorp Genetics (formerly Invitae), Labcorp RCV002286174 SCV003787866 likely benign not provided 2024-02-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003454071 SCV004183039 likely benign Retinitis pigmentosa 39 2023-11-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003454070 SCV004183040 likely benign Usher syndrome type 2A 2023-11-04 criteria provided, single submitter clinical testing

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