ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.40133C>T (p.Pro13378Leu)

dbSNP: rs2062187429
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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 RCV001093551 SCV000999102 likely benign Hypertrophic cardiomyopathy criteria provided, single submitter research

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