ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.107696T>C (p.Ile35899Thr)

gnomAD frequency: 0.00006  dbSNP: rs372276487
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Genomics Program, Sidra Medicine RCV001293128 SCV001434118 likely benign Primary dilated cardiomyopathy criteria provided, single submitter research
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799057 SCV002042348 uncertain significance Cardiomyopathy 2019-12-04 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003142229 SCV003826645 uncertain significance not provided 2022-09-20 criteria provided, single submitter clinical testing

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