ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.27677G>A (p.Cys9226Tyr)

gnomAD frequency: 0.00001  dbSNP: rs369108107
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV000171322 SCV000221519 likely pathogenic not provided criteria provided, single submitter research
Eurofins Ntd Llc (ga) RCV000171322 SCV000701203 uncertain significance not provided 2017-04-19 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003155102 SCV003844514 uncertain significance not specified 2023-02-10 criteria provided, single submitter clinical testing

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