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Sensitive

Diverticular disease

TNS1 · rs1427669

Where this position leads

Condition: Diverticular Disease

rs1427669 Condition: Diverticular Disease Diverticular Disease Condition rs1427669 rs1427669 TNS1

What the study found

Who was studied 56,355 European ancestry cases, 398,413 European ancestry controls.

The effect Each copy of the T allele shifted the measure 0.05 higher (95% confidence interval 0.036-0.064); p = 4 × 10−14.

How common The T allele had a frequency of about 76% in the people studied.

Where it sits Chromosome 2, band 2q35 — in an intron of TNS1.

What each result means

G/G Published research associates this genotype with typical/baseline likelihood of Diverticular disease — no copies of the reported risk allele.
G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Diverticular disease.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Diverticular disease compared to the general population.
Source
150 risk variants for diverticular disease of intestine prioritize cell types and enable polygenic prediction of disease susceptibility
Wu Y, Goleva SB, Breidenbach LB, Kim M, MacGregor S, Gandal MJ, Davis LK, Wray NR
Cell genomics · 2023 · PMID 37492107 · open access

Questions about rs1427669

What is rs1427669?

rs1427669 is a single position in the genome, in or near the TNS1 gene. Published research associates it with diverticular disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1427669 linked to?

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

Does having rs1427669 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 rs1427669 come from?

GWAS Catalog, Cell genomics 2023, PMID:37492107. 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.

Diverticular disease (rs1427669). MyGeneLog™. https://www.mygenelog.com/variants/rs1427669

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