ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.30485C>A (p.Thr10162Lys)

dbSNP: rs200593368
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799173 SCV002042429 uncertain significance Cardiomyopathy 2019-06-10 criteria provided, single submitter clinical testing

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