Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000156357 | SCV000206075 | likely benign | not specified | 2014-02-07 | criteria provided, single submitter | clinical testing | 590+13G>A in Intron 4 of MYH14: This variant is not expected to have clinical si gnificance because it is not located within the splice consensus sequence and is not predicted to impact splicing. |