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High light scatter reticulocyte percentage of red cells

near F2R · rs144215134

Where this position leads

Condition: Blood Cell Counts

rs144215134 Condition: Blood Cell Counts Blood Cell Counts Condition rs144215134 rs144215134 near F2R

What the study found

Who was studied 170,763 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0651 (percentage) higher (95% confidence interval 0.049-0.082); p = 1 × 10−14.

How common The C allele had a frequency of about 5% in the people studied.

Where it sits Chromosome 5, band 5q13.3 — between genes, 10.9 kb from LOC124901199.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of High light scatter reticulocyte percentage of red cells — no copies of the reported risk allele.
A/C Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with High light scatter reticulocyte percentage of red cells.
C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of High light scatter reticulocyte percentage of red cells compared to the general population.
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 rs144215134

What is rs144215134?

rs144215134 is a single position in the genome, in or near the near F2R gene. Published research associates it with high light scatter reticulocyte percentage of red cells. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs144215134 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 rs144215134 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 rs144215134 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.

Quoting this page

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.

High light scatter reticulocyte percentage of red cells (rs144215134). MyGeneLog™. https://www.mygenelog.com/variants/rs144215134

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