Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000036851 | SCV000060506 | likely benign | not specified | 2011-10-12 | criteria provided, single submitter | clinical testing | 756-15_756-12delCTCT in intron 7 of LDB3: This variant is not expected to have c linical significance because it is not located in the conserved +/- 1, 2 region of the splicing consensus sequence. |
Eurofins Ntd Llc |
RCV000036851 | SCV000332565 | benign | not specified | 2015-07-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001668154 | SCV001883480 | benign | not provided | 2019-08-13 | criteria provided, single submitter | clinical testing |