ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.58775C>A (p.Thr19592Asn)

dbSNP: rs745441183
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000503640 SCV000597692 uncertain significance not specified 2016-09-02 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003150247 SCV003838594 uncertain significance Cardiomyopathy 2021-09-22 criteria provided, single submitter clinical testing

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