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Body shape phenotype PC2

near DYNLT3P2 · rs17262146

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 460,198 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.014 lower (95% confidence interval 0.0097-0.0183); p = 2 × 10⁻¹⁰.

How common The A allele had a frequency of about 58% in the people studied.

Where it sits Chromosome 2, band 2q14.3 — between genes, 0.5 kb from DYNLT3P2.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Body shape phenotype PC2 compared to the general population.

A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Body shape phenotype PC2.

G/G Published research associates this genotype with typical/baseline likelihood of Body shape phenotype PC2 — no copies of the reported risk allele.

Source

Tissue-specific genetic variation suggests distinct molecular pathways between body shape phenotypes and colorectal cancer

Peruchet-Noray L, Sedlmeier AM, Dimou N, Baurecht H, Fervers B, Fontvieille E, Konzok J, Tsilidis KK, Christakoudi S, Jansana A, Cordova R, Bohmann P

and 18 more — show all

Stein MJ, Weber A, Bézieau S, Brenner H, Chan AT, Cheng I, Figueiredo JC, Garcia-Etxebarria K, Moreno V, Newton CC, Schmit SL, Song M, Ulrich CM, Ferrari P, Viallon V, Carreras-Torres R, Gunter MJ, Freisling H

Science advances · 2024 · PMID 38640244 · open access

Questions about rs17262146

What is rs17262146?

rs17262146 is a single position in the genome, in or near the near DYNLT3P2 gene. Published research associates it with body shape phenotype pc2. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs17262146 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 rs17262146 come from?

GWAS Catalog, Science advances 2024, PMID:38640244. 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.

Body shape phenotype PC2 (rs17262146). MyGeneLog™. https://www.mygenelog.com/variants/rs17262146

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