ClinVar Miner

Submissions for variant NM_019098.5(CNGB3):c.212-2527_338+2854del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory, Institute for Ophthalmic Research RCV000497979 SCV000575862 pathogenic Achromatopsia 3 2017-03-27 no assertion criteria provided research

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