Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000604258 | SCV000713712 | likely benign | not specified | 2017-10-05 | criteria provided, single submitter | clinical testing | p.Lys4674Lys in exon 69 of GPR98: This variant is not expected to have clinical significance because it does not alter an amino acid residue and is not located within the splice consensus sequence. ACMG/AMP Criteria applied: BP7 (Richards 2 015). |
Invitae | RCV003767457 | SCV004626905 | likely benign | not provided | 2023-11-10 | criteria provided, single submitter | clinical testing |