ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.48160+19del

dbSNP: rs2154208221
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Academic Medical Center RCV001700575 SCV001921687 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001726663 SCV001965682 likely benign not provided no assertion criteria provided clinical testing

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