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Ascending aorta maximum area

LINC02269 · rs67846163

What the study found

Who was studied 32,590 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 16.3 lower; p = 6 × 10−31.

How common The A allele had a frequency of about 77% in the people studied.

Where it sits Chromosome 4, band 4q34.1 — in an intron of LINC02269.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Ascending aorta maximum area compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Ascending aorta maximum area.
G/G Published research associates this genotype with typical/baseline likelihood of Ascending aorta maximum area — no copies of the reported risk allele.
Source

Questions about rs67846163

What is rs67846163?

rs67846163 is a single position in the genome, in or near the LINC02269 gene. Published research associates it with ascending aorta maximum area. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs67846163 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 rs67846163 come from?

GWAS Catalog, Nature communications 2022, PMID:35922433. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Ascending aorta maximum area (rs67846163). MyGeneLog™. https://www.mygenelog.com/variants/rs67846163

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