Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000039534 | SCV000063223 | likely benign | not specified | 2012-09-22 | criteria provided, single submitter | clinical testing | 1509+11T>C in intron 8 of GPR98: This variant is not expected to have clinical s ignificance because it is not located within the conserved region of the splice consensus sequence. |
Invitae | RCV003546464 | SCV004265838 | likely benign | not provided | 2023-07-09 | criteria provided, single submitter | clinical testing |