ClinVar Miner

Submissions for variant NC_000001.10:g.155183259_(155210558_155210826)del

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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, University of Leipzig Medical Center RCV002468859 SCV002765045 likely pathogenic Parkinson disease, late-onset 2022-12-19 criteria provided, single submitter clinical testing _x000D_ Criteria applied: PVS1, PS4_MOD

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