LINC02929 · rs112017605
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 158 European ancestry postmortem cases, 1,263 European ancestry postmortem controls.
The effect Each copy of the A allele carried 3.01 times the odds of Lewy body pathology (95% confidence interval 2.03-4.06); p = 5 × 10−10.
How common The A allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 10, band 10q21.2 — in an intron of LINC02929.
rs112017605 is a single position in the genome, in or near the LINC02929 gene. Published research associates it with lewy body pathology. 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, Acta neuropathologica communications 2023, PMID:37700353. 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.
Lewy body pathology (rs112017605). MyGeneLog™. https://www.mygenelog.com/variants/rs112017605