ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.719+12_719+28del

dbSNP: rs2526938952
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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 RCV003150656 SCV003838077 uncertain significance Cardiomyopathy 2022-05-20 criteria provided, single submitter clinical testing

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