ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.54327del (p.Lys18110fs)

dbSNP: rs2054381012
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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 RCV001093579 SCV000999121 likely pathogenic Primary dilated cardiomyopathy criteria provided, single submitter research

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