C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Serum uric acid levels compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Serum uric acid levels.
T/TPublished research associates this genotype with typical/baseline likelihood of Serum uric acid levels — no copies of the reported risk allele.
BMC medical genomics · 2014 · PMID 24513273 · open access
Questions about rs4148152
What is rs4148152?
rs4148152 is a single position in the genome, in or near the ABCG2 gene. Published research associates it with serum uric acid levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does rs4148152 affect how medicines work?
ABCG2 carries pharmacogenomic findings for Statins. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.
Does having rs4148152 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs4148152 come from?
GWAS Catalog, BMC Med Genomics 2014, PMID:24513273. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.