CLIC2 · rs151113194
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 1,238,180 European, East Asian, Hispanic, admixed African or South Asian ancestry individuals; replicated in 1,236 Arab ancestry individuals, 4,362 Asian ancestry individuals, 8,205 Hispanic individuals, 10,657 African ancestry individuals, 22,967 African American individuals, 28,290 South Asian ancestry individuals, 71,410 European ancestry individuals, 160,212 East Asian ancestry individuals.
The effect Each copy of the T allele shifted the measure 0.0177 higher (95% confidence interval 0.012-0.023); p = 3 × 10−11.
How common The T allele had a frequency of about 7% in the people studied.
Where it sits Chromosome X, band Xq28 — in an intron of CLIC2.
rs151113194 is a single position in the genome, in or near the CLIC2 gene. Published research associates it with high density lipoprotein cholesterol levels. 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, Genome biology 2022, PMID:36575460. 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.
High density lipoprotein cholesterol levels (rs151113194). MyGeneLog™. https://www.mygenelog.com/variants/rs151113194