LINC02767 · rs11118962
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 119,330 African American or Afro-Caribbean individuals, 57,986 Hispanic or Latin American individuals, 6,419 East Asian ancestry individuals, 425,720 European ancestry individuals.
The effect Each copy of the T allele shifted the measure 0.0355 higher (95% confidence interval 0.03-0.041); p = 9 × 10−39.
How common The T allele had a frequency of about 69% in the people studied.
Where it sits Chromosome 1, band 1q32.2 — in an intron of LINC02767.
rs11118962 is a single position in the genome, in or near the LINC02767 gene. Published research associates it with heart rate (hr, minimum, inv-normal transformed). 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, Science (New York, N.Y.) 2024, PMID:39024449. 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.
heart rate (HR, minimum, inv-normal transformed) (rs11118962). MyGeneLog™. https://www.mygenelog.com/variants/rs11118962