ClinVar Miner

Submissions for variant NC_000001.11:g.222617967_222617972del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003414786 SCV004125657 likely benign not provided 2022-12-01 criteria provided, single submitter clinical testing MIA3: BS2

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