Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
ARUP Laboratories, |
RCV003120152 | SCV003799806 | uncertain significance | not provided | 2022-06-30 | criteria provided, single submitter | clinical testing | The PIEZO1 c.4556A>C; p.Gln1519Pro variant (rs767365106) is reported in the literature in individuals affected with hereditary xerocytosis (Picard 2019) or hydrops fetalis (Al-Kouatly 2021), but without clear association with disease. This variant is found in the general population with an overall allele frequency of 0.037% (67/181532 alleles) in the Genome Aggregation Database. The glutamine at codon 1519 is weakly conserved, and computational analyses are uncertain whether this variant is neutral or deleterious (REVEL: 0.560). Due to limited information, the clinical significance of this variant is uncertain at this time. References: Al-Kouatly HB et al. High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study. Genet Med. 2021 Jul;23(7):1325-1333. PMID: 33686258. Picard V et al. Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients. Haematologica. 2019 Aug;104(8):1554-1564. PMID: 30655378. |
Revvity Omics, |
RCV003120152 | SCV003813022 | uncertain significance | not provided | 2023-12-27 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV003333240 | SCV004041024 | uncertain significance | Lymphatic malformation 6 | 2023-06-05 | criteria provided, single submitter | clinical testing | |
Mayo Clinic Laboratories, |
RCV003120152 | SCV005412532 | uncertain significance | not provided | 2024-01-25 | criteria provided, single submitter | clinical testing | BP4 |