Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Illumina Laboratory Services, |
RCV000291982 | SCV000426375 | uncertain significance | Pulmonary hypertension, primary, 1 | 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. |
| Invitae | RCV002521363 | SCV003006542 | uncertain significance | Primary pulmonary hypertension | 2022-04-13 | criteria provided, single submitter | clinical testing | This variant occurs in a non-coding region of the BMPR2 gene. It does not change the encoded amino acid sequence of the BMPR2 protein. This variant is not present in population databases (gnomAD no frequency). This variant has been observed in individual(s) with pulmonary arterial hypertension (PMID: 26699722). ClinVar contains an entry for this variant (Variation ID: 333630). 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. |