ClinVar Miner

Submissions for variant NM_130837.3(OPA1):c.1889A>T (p.Glu630Val)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Division of Molecular and Cellular Biology, National Hospital Organization Tokyo Medical Center RCV003164467 SCV002581966 uncertain significance Autosomal dominant optic atrophy classic form 2022-09-01 no assertion criteria provided research

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