Sensitive

Asthma-COPD overlap syndrome

near ERBB3 · rs7312770

Where this position leads

Condition: Asthma

rs7312770 Condition: Asthma Asthma Condition rs7312770 rs7312770 near ERBB3

What the study found

Who was studied 8,068 European ancestry cases, 40,360 European ancestry controls; replicated in 4,301 European ancestry cases, 48,609 European ancestry controls, 297 African American cases, 1,335 African American controls.

The effect Each copy of the T allele carried 0.91 times the odds of Asthma-COPD overlap syndrome (95% confidence interval 0.883-0.937); p = 5 × 10−10.

How common The T allele had a frequency of about 50% in the people studied.

Where it sits Chromosome 12, band 12q13.2 — between genes, 3 kb from ERBB3.

What each result means

C/C No copy of the version the research linked to Asthma-COPD overlap syndrome. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Asthma-COPD overlap syndrome. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Asthma-COPD overlap syndrome. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs7312770

What is rs7312770?

rs7312770 is a single position in the genome, in or near the near ERBB3 gene. Published research associates it with asthma-copd overlap syndrome. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7312770 linked to?

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

Does having rs7312770 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 rs7312770 come from?

GWAS Catalog, Chest 2022, PMID:35104449. 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.

Asthma-COPD overlap syndrome (rs7312770). MyGeneLog™. https://www.mygenelog.com/variants/rs7312770

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