Standard
Eotaxin levels
near GASK1A · rs116826172
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 each result means
C/C
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Eotaxin levels compared to the general population.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Eotaxin levels.
T/T
Published research associates this genotype with typical/baseline likelihood of Eotaxin levels — no copies of the reported risk allele.
Source
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors
Ahola-Olli AV,
Würtz P,
Havulinna AS,
Aalto K,
Pitkänen N,
Lehtimäki T,
Kähönen M,
Lyytikäinen LP,
Raitoharju E,
Seppälä I,
Sarin AP,
Ripatti S
and 9 more — show all
American journal of human genetics · 2017 · PMID 27989323
Questions about rs116826172
What is rs116826172?
rs116826172 is a single position in the genome, in or near the near GASK1A gene. Published research associates it with eotaxin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs116826172 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 rs116826172 come from?
GWAS Catalog, Am J Hum Genet 2016, PMID:27989323. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants