ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.68314G>C (p.Gly22772Arg)

dbSNP: rs1559480997
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000729687 SCV000857373 uncertain significance not provided 2017-10-06 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003230581 SCV003928663 uncertain significance not specified 2023-04-04 criteria provided, single submitter clinical testing

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