ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.93908T>C (p.Val31303Ala)

dbSNP: rs1697801738
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001558861 SCV001780890 likely benign not provided 2019-07-30 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001558861 SCV005050677 uncertain significance not provided 2024-05-01 criteria provided, single submitter clinical testing TTN: PM2

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