Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000156603 | SCV000206322 | likely benign | not specified | 2014-06-18 | criteria provided, single submitter | clinical testing | 799+14G>C in intron 9 of MYH6: This variant is not expected to have clinical sig nificance because it is not located within the splice consensus sequence. |