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Ascending aorta maximum area

near HMCN1 · rs34923020

What the study found

Who was studied 32,590 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 7.77 lower; p = 5 × 10−9.

How common The G allele had a frequency of about 73% in the people studied.

Where it sits Chromosome 1, band 1q25.3 — between genes, 8.2 kb from HMCN1.

What each result means

A/A No copy of the version the research linked to Ascending aorta maximum area. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Ascending aorta maximum area. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Ascending aorta maximum area. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs34923020

What is rs34923020?

rs34923020 is a single position in the genome, in or near the near HMCN1 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 rs34923020 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 rs34923020 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

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.

Ascending aorta maximum area (rs34923020). MyGeneLog™. https://www.mygenelog.com/variants/rs34923020

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