ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.66553G>A (p.Gly22185Ser)

gnomAD frequency: 0.00002  dbSNP: rs560206502
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003137472 SCV003819120 uncertain significance not provided 2020-08-27 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV003137472 SCV004225828 uncertain significance not provided 2022-02-14 criteria provided, single submitter clinical testing

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