Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000216102 | SCV000271022 | likely benign | not specified | 2015-12-04 | criteria provided, single submitter | clinical testing | c.36310+15A>C in intron 186 of TTN: This variant is not expected to have clinica l significance because it is not located within the splice consensus sequence. |