ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.8902+13_8902+14delinsGA

dbSNP: rs1553993564
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000615385 SCV000731666 likely benign not specified 2017-05-19 criteria provided, single submitter clinical testing c.8902+13_8902+14delinsGA in intron 37 of TTN: This variant is not expected to h ave clinical significance because it is not located within the splice consensus sequence.

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