Sensitive

Chronic obstructive pulmonary disease

FGD6 · rs60129850

Where this position leads

Condition: Chronic Obstructive Pulmonary Disease (COPD)

rs60129850 Condition: Chronic Obstructive Pulmonary Disease (COPD) Chronic Obstructive Pulmonary Disea… Condition rs60129850 rs60129850 FGD6

What the study found

Who was studied 35,735 cases, 222,076 controls.

The effect Each copy of the A allele carried 1.07 times the odds of Chronic obstructive pulmonary disease; p = 2 × 10−8.

How common The A allele had a frequency of about 21% in the people studied.

Where it sits Chromosome 12, band 12q22 — in an intron of FGD6.

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/C One copy of the version the research linked to Chronic obstructive pulmonary disease. That is a smaller link than two copies.
C/C 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 rs60129850

What is rs60129850?

rs60129850 is a single position in the genome, in or near the FGD6 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 rs60129850 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 rs60129850 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 rs60129850 come from?

GWAS Catalog, Nature genetics 2019, PMID:30804561. 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 (rs60129850). MyGeneLog™. https://www.mygenelog.com/variants/rs60129850

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