ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.4852+1G>A

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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 RCV001199713 SCV001162553 pathogenic Usher syndrome type 1 2020-01-09 criteria provided, single submitter research

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