Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Labcorp Genetics |
RCV003078810 | SCV003474263 | uncertain significance | Leukocyte adhesion deficiency 1 | 2023-08-17 | criteria provided, single submitter | clinical testing | In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) has been performed at Invitae for this missense variant, however the output from this modeling did not meet the statistical confidence thresholds required to predict the impact of this variant on ITGB2 protein function. ClinVar contains an entry for this variant (Variation ID: 2161910). This sequence change replaces methionine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 762 of the ITGB2 protein (p.Met762Arg). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with ITGB2-related conditions. |
| Center for Genomic Medicine, |
RCV003078810 | SCV005374377 | uncertain significance | Leukocyte adhesion deficiency 1 | 2024-09-22 | criteria provided, single submitter | clinical testing |