ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.70274G>C (p.Ser23425Thr)

dbSNP: rs980974415
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Genomics Program, Sidra Medicine RCV001093576 SCV000999118 likely benign Primary dilated cardiomyopathy criteria provided, single submitter research
Breakthrough Genomics, Breakthrough Genomics RCV004711308 SCV005259439 likely benign not provided criteria provided, single submitter not provided

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