Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Clin |
RCV000283041 | SCV004037423 | uncertain significance | Glanzmann thrombasthenia | 2023-08-15 | reviewed by expert panel | curation | The variant NM_000419.5(ITGA2B):c.945+10A>G has not been reported in the literature. It has previously been submitted to ClinVar (SCV000403381.3) however the affected status of the individual is unkown. The variant is absent from gnomAD (PM2_supporting). Meanwhile, the in silico predictor splice AI predics no impact on splicing and the variant occurs at a nucleotide position that is not highly conserved (BP7). In summary, this variant meets the criteria to be classified as variant of uncertain significance for autosomal recessive Glanzmann Thrombasthenia based on the ACMG/AMP criteria applied, as specified by the ClinGen PD VCEP: PM2_supporting and BP7 (PD VCEP specifications version 2.1). |
Illumina Laboratory Services, |
RCV000283041 | SCV000403381 | uncertain significance | Glanzmann thrombasthenia | 2018-01-13 | criteria provided, single submitter | clinical testing | This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease. |