ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.42439C>T (p.Pro14147Ser)

dbSNP: rs1559970037
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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 RCV000714031 SCV000844694 uncertain significance not provided 2018-05-24 criteria provided, single submitter clinical testing
New York Genome Center RCV003448339 SCV004176047 uncertain significance Dilated cardiomyopathy 1G; Hypertrophic cardiomyopathy 9 2023-05-04 criteria provided, single submitter clinical testing

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