ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.67534G>T (p.Asp22512Tyr)

dbSNP: rs786205540
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Total submissions: 2
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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 RCV000171316 SCV000221513 likely benign not specified 2016-09-28 criteria provided, single submitter research
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003486719 SCV004240070 likely benign Cardiomyopathy 2023-05-16 criteria provided, single submitter clinical testing

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