ClinVar Miner

Submissions for variant NM_003816.3:c.333+2_1303del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Genetics in Ophthalmology, Institut Imagine RCV003319560 SCV004023367 uncertain significance Cone-rod dystrophy 9 no assertion criteria provided research

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