ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.82112G>A (p.Gly27371Glu)

gnomAD frequency: 0.00003  dbSNP: rs766785319
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001592466 SCV001824111 uncertain significance not provided 2019-05-20 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001592466 SCV003826014 uncertain significance not provided 2019-12-02 criteria provided, single submitter clinical testing

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