ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.13709G>C (p.Arg4570Pro)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg RCV004817274 SCV005070523 uncertain significance Retinal dystrophy 2016-01-01 no assertion criteria provided clinical testing

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