ClinVar Miner

Submissions for variant NM_174878.3(CLRN1):c.433+1109C>A

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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 RCV004815905 SCV005070202 uncertain significance Retinal dystrophy 2022-01-01 no assertion criteria provided clinical testing

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