ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.2842-111C>A

gnomAD frequency: 0.04999  dbSNP: rs2306637
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 RCV001665788 SCV001881225 benign not provided 2018-06-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001665788 SCV005241419 benign not provided criteria provided, single submitter not provided

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