ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.54483A>C (p.Gln18161His)

dbSNP: rs1559711872
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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 RCV000768994 SCV000900367 uncertain significance Cardiomyopathy 2016-08-04 criteria provided, single submitter clinical testing

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