Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000217560 | SCV000270032 | likely benign | not specified | 2015-06-25 | criteria provided, single submitter | clinical testing | p.2289+11_2289+12delinsCT in intron 21 of CDH23: This variant is not expected to have clinical significance because it is not located within the splice consensu s sequence. |