ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.34175C>T (p.Pro11392Leu)

dbSNP: rs868108980
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702282 SCV001931896 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001702282 SCV001952281 likely benign not provided no assertion criteria provided clinical testing

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