ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.21674T>C (p.Phe7225Ser)

gnomAD frequency: 0.00001  dbSNP: rs780534846
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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 RCV000516399 SCV000616023 uncertain significance not provided 2017-07-11 criteria provided, single submitter clinical testing
Genetics and Genomics Program, Sidra Medicine RCV001293143 SCV001434133 uncertain significance Hypertrophic cardiomyopathy criteria provided, single submitter research

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