ClinVar Miner

Submissions for variant NM_001194.4(HCN2):c.1087G>A (p.Ala363Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003322065 SCV004026108 uncertain significance not provided 2022-07-20 criteria provided, single submitter clinical testing

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