ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.13709del (p.Arg4570fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV004573821 SCV005055688 likely pathogenic Retinitis pigmentosa 39 2024-03-16 criteria provided, single submitter clinical testing

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