ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.91+55A>G

gnomAD frequency: 0.01610  dbSNP: rs72647841
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 RCV001648770 SCV001861895 benign not provided 2018-06-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001648770 SCV005241435 benign not provided criteria provided, single submitter not provided

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