ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.35471-51C>T

gnomAD frequency: 0.01630  dbSNP: rs150597207
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 RCV001589806 SCV001815277 likely benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001589806 SCV005259997 likely benign not provided criteria provided, single submitter not provided

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