ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.23099-6T>C

dbSNP: rs1560672202
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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 RCV000770072 SCV000901498 uncertain significance Cardiomyopathy 2016-05-05 criteria provided, single submitter clinical testing

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