ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.96919G>A (p.Asp32307Asn)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003143083 SCV003822808 uncertain significance not provided 2022-08-29 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003150588 SCV003837956 likely benign Cardiomyopathy 2022-06-24 criteria provided, single submitter clinical testing

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