ClinVar Miner

Submissions for variant NM_020843.4(SCAPER):c.2544T>G (p.Ile848Met)

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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 RCV004817620 SCV005069491 uncertain significance Optic atrophy 2023-01-01 no assertion criteria provided clinical testing

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