ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.95798C>T (p.Pro31933Leu)

dbSNP: rs769829272
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000517505 SCV000616187 uncertain significance not specified 2017-04-12 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003486855 SCV004240186 likely benign Cardiomyopathy 2023-03-06 criteria provided, single submitter clinical testing

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