ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.29694+21A>T

gnomAD frequency: 0.00110  dbSNP: rs187393718
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001583510 SCV001812472 likely benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001583510 SCV005260030 likely benign not provided criteria provided, single submitter not provided

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