ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.63571C>A (p.Pro21191Thr)

dbSNP: rs2049345864
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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 RCV001093577 SCV000999119 likely benign Primary dilated cardiomyopathy criteria provided, single submitter research

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