ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.38381-8C>G

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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 RCV003884844 SCV004701855 likely benign not provided 2024-01-01 criteria provided, single submitter clinical testing TTN: BP4

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