Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000219423 | SCV000271163 | likely benign | not specified | 2015-10-02 | criteria provided, single submitter | clinical testing | p.Ser669Ser in exon 12 of USH2A: This variant is not expected to have clinical s ignificance because it does not alter an amino acid residue and is not located w ithin the splice consensus sequence. |