ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.40574C>G (p.Pro13525Arg)

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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 RCV003429415 SCV004152435 uncertain significance not provided 2022-09-01 criteria provided, single submitter clinical testing

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