Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000615385 | SCV000731666 | likely benign | not specified | 2017-05-19 | criteria provided, single submitter | clinical testing | c.8902+13_8902+14delinsGA in intron 37 of TTN: This variant is not expected to h ave clinical significance because it is not located within the splice consensus sequence. |