ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.95029T>C (p.Phe31677Leu)

dbSNP: rs1559147244
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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 RCV000768852 SCV000900225 uncertain significance Cardiomyopathy 2016-05-04 criteria provided, single submitter clinical testing

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