ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.77203G>A (p.Val25735Met)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, Skane University Hospital Lund RCV004698205 SCV005198902 uncertain significance not provided 2024-02-12 criteria provided, single submitter clinical testing

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