Sensitive

Chronic obstructive pulmonary disease

CYP2B7P · rs73038469

Where this position leads

Condition: Chronic Obstructive Pulmonary Disease (COPD)

rs73038469 Condition: Chronic Obstructive Pulmonary Disease (COPD) Chronic Obstructive Pulmonary Disea… Condition rs73038469 rs73038469 CYP2B7P

What the study found

Who was studied 4,017 East Asian ancestry cases, 162,653 East Asian ancestry controls.

The effect Each copy of the A allele shifted the measure 0.317 higher (95% confidence interval 0.25-0.38); p = 1 × 10−20.

How common The A allele had a frequency of about 17% in the people studied.

Where it sits Chromosome 19, band 19q13.2 — in an intron of CYP2B7P.

What each result means

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

Questions about rs73038469

What is rs73038469?

rs73038469 is a single position in the genome, in or near the CYP2B7P gene. Published research associates it with chronic obstructive pulmonary 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 rs73038469 linked to?

On MyGeneLog this position is linked to Chronic Obstructive Pulmonary Disease (COPD). The research behind each link, and its sources, are set out on that condition page.

Does having rs73038469 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 rs73038469 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. 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.

Chronic obstructive pulmonary disease (rs73038469). MyGeneLog™. https://www.mygenelog.com/variants/rs73038469

← See all variants