ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.31473G>A (p.Met10491Ile)

dbSNP: rs780137093
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Total submissions: 2
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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 RCV001799174 SCV002042433 uncertain significance Cardiomyopathy 2019-05-13 criteria provided, single submitter clinical testing
Baylor Genetics RCV004558653 SCV005049458 uncertain significance Tibial muscular dystrophy 2024-03-28 criteria provided, single submitter clinical testing

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