Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001184538 | SCV001350544 | uncertain significance | Familial hypercholesterolemia | 2022-11-08 | criteria provided, single submitter | clinical testing | This missense variant (also known as p.Glu359Lys in the mature protein) replaces glutamic acid with lysine at codon 380 of the LDLR protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with LDLR-related disorders in the literature. This variant has been identified in 1/31406 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance. |
Fulgent Genetics, |
RCV002491540 | SCV002781090 | uncertain significance | Hypercholesterolemia, familial, 1 | 2021-10-25 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV002491540 | SCV004820271 | uncertain significance | Hypercholesterolemia, familial, 1 | 2024-07-10 | criteria provided, single submitter | clinical testing | This missense variant (also known as p.Glu359Lys in the mature protein) replaces glutamic acid with lysine at codon 380 of the LDLR protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with familial hypercholesterolemia in the literature. This variant has been identified in 1/31406 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance. |