TRIM2 · rs6827197
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 306 Chinese ancestry male cases, 3,516 Chinese ancestry controls.
The effect The reported allele is T; the catalogue records no effect size ; p = 2 × 10−9.
How common The T allele had a frequency of about 3% in the people studied.
Where it sits Chromosome 4, band 4q31.3 — between genes, 36.8 kb from TRIM2.
rs6827197 is a single position in the genome, in or near the TRIM2 gene. Published research associates it with thyrotoxic periodic paralysis. 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, European journal of endocrinology 2020, PMID:33105104. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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Thyrotoxic periodic paralysis (rs6827197). MyGeneLog™. https://www.mygenelog.com/variants/rs6827197