ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.59920C>A (p.Pro19974Thr)

gnomAD frequency: 0.00001  dbSNP: rs778877970
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Genomics Program, Sidra Medicine RCV001293176 SCV001434174 likely benign Primary dilated cardiomyopathy criteria provided, single submitter research

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