Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000215697 | SCV000270226 | likely benign | not specified | 2015-05-07 | criteria provided, single submitter | clinical testing | p.Ile4218Ile in exon 62 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. |
Invitae | RCV001462013 | SCV001665924 | likely benign | not provided | 2022-08-31 | criteria provided, single submitter | clinical testing |