RIN3 · rs76688721
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 47,745 European ancestry individuals.
The effect Each copy of the G allele shifted the measure 0.247 higher (95% confidence interval 0.18-0.31); p = 3 × 10−15.
How common The G allele had a frequency of about 1% in the people studied.
Where it sits Chromosome 14, band 14q32.12 — in an intron of RIN3.
rs76688721 is a single position in the genome, in or near the RIN3 gene. Published research associates it with lgmn protein 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, Nature genetics 2025, PMID:39789286. 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.
LGMN protein levels (rs76688721). MyGeneLog™. https://www.mygenelog.com/variants/rs76688721