SLC22A12 · rs75786299
Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 42,378 Korean ancestry individuals.
The effect Each copy of the A allele carried 3.00 times the odds of Hyperuricemia in low cholesterol intake (95% confidence interval 2.47-3.65); p = 3 × 10−28.
Where it sits Chromosome 11, band 11q13.1 — in an intron of SLC22A12.
What ClinVar records
Classification
Benign/Likely benign for Dalmatian hypouricemia; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2025-12-30.
ClinVar record 880049 NM_144585.4(SLC22A12):c.661+11G>A
What this is ClinVar's aggregate record for this position (as of its 2026-09-24 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.
rs75786299 is a single position in the genome, in or near the SLC22A12 gene. Published research associates it with hyperuricemia in low cholesterol intake. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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.
GWAS Catalog, Scientific reports 2025, PMID:40835619. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Hyperuricemia in low cholesterol intake (rs75786299). MyGeneLog™. https://www.mygenelog.com/variants/rs75786299