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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 8,809 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.244 lower (95% confidence interval 0.17-0.32); p = 4 × 10−11.
Where it sits Chromosome 6, band 6p21.33 — in an intron of TNXB.
What each result means
C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of X-11470 levels compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with X-11470 levels.
T/TPublished research associates this genotype with typical/baseline likelihood of X-11470 levels — no copies of the reported risk allele.
rs17201560 is a single position in the genome, in or near the TNXB gene. Published research associates it with x-11470 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17201560 mean I will get this?
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.
Where does the information about rs17201560 come from?
GWAS Catalog, Metabolites 2022, PMID:35050183. 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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