Gene Knowledge Graph
UTC
Standard

Eosinophil count

PVT1 · rs11786130

Where this position leads

Condition: Blood Cell Counts

rs11786130 Condition: Blood Cell Counts Blood Cell Counts Condition rs11786130 rs11786130 PVT1

What the study found

Who was studied 172,275 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0352 lower (95% confidence interval 0.028-0.043); p = 7 × 10−21.

How common The A allele had a frequency of about 35% in the people studied.

Where it sits Chromosome 8, band 8q24.21 — in an intron of PVT1.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Eosinophil count compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Eosinophil count.
G/G Published research associates this genotype with typical/baseline likelihood of Eosinophil count — no copies of the reported risk allele.
Source
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Astle WJ, Elding H, Jiang T, Allen D, Ruklisa D, Mann AL, Mead D, Bouman H, Riveros-Mckay F, Kostadima MA, Lambourne JJ, Sivapalaratnam S
and 62 more — show all
Downes K, Kundu K, Bomba L, Berentsen K, Bradley JR, Daugherty LC, Delaneau O, Freson K, Garner SF, Grassi L, Guerrero J, Haimel M, Janssen-Megens EM, Kaan A, Kamat M, Kim B, Mandoli A, Marchini J, Martens JHA, Meacham S, Megy K, O'Connell J, Petersen R, Sharifi N, Sheard SM, Staley JR, Tuna S, van der Ent M, Walter K, Wang SY, Wheeler E, Wilder SP, Iotchkova V, Moore C, Sambrook J, Stunnenberg HG, Di Angelantonio E, Kaptoge S, Kuijpers TW, Carrillo-de-Santa-Pau E, Juan D, Rico D, Valencia A, Chen L, Ge B, Vasquez L, Kwan T, Garrido-Martín D, Watt S, Yang Y, Guigo R, Beck S, Paul DS, Pastinen T, Bujold D, Bourque G, Frontini M, Danesh J, Roberts DJ, Ouwehand WH, Butterworth AS, Soranzo N
Cell · 2016 · PMID 27863252 · open access

Questions about rs11786130

What is rs11786130?

rs11786130 is a single position in the genome, in or near the PVT1 gene. Published research associates it with eosinophil count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11786130 linked to?

On MyGeneLog this position is linked to Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.

Does having rs11786130 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 rs11786130 come from?

GWAS Catalog, Cell 2016, PMID:27863252. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

← See all variants