ClinVar Miner

Submissions for variant NC_000019.10:g.11089455G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004012070 SCV004824544 uncertain significance Hypercholesterolemia, familial, 1 2024-07-29 criteria provided, single submitter clinical testing This variant causes a single nucleotide change in the sterol-independent regulatory element in the promoter region of the LDLR gene. 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 1/31390 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.

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