ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.90298G>C (p.Glu30100Gln)

dbSNP: rs762287310
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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 RCV001700947 SCV001927062 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001700947 SCV001957392 likely benign not provided no assertion criteria provided clinical testing

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