Sensitive

Allergic disease (asthma, hay fever or eczema)

MFSD13A · rs10883723

Where this position leads

Condition: Asthma

rs10883723 Condition: Asthma Asthma Condition rs10883723 rs10883723 MFSD13A

What the study found

Who was studied 106,772 European ancestry cases, 239,773 European ancestry controls; replicated in 83,335 cases, 34,934 controls.

The effect Each copy of the C allele carried 1.03 times the odds of Allergic disease (asthma, hay fever or eczema) (95% confidence interval 1.024-1.046); p = 1 × 10−9.

How common The C allele had a frequency of about 36% in the people studied.

Where it sits Chromosome 10, band 10q24.32 — in the 5′ untranslated region of MFSD13A.

What each result means

C/C Two copies of the version the research linked to Allergic disease (asthma, hay fever or eczema). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Allergic disease (asthma, hay fever or eczema). That is a smaller link than two copies.
T/T No copy of the version the research linked to Allergic disease (asthma, hay fever or eczema). This is the starting point the study compared everyone against.
Source

Questions about rs10883723

What is rs10883723?

rs10883723 is a single position in the genome, in or near the MFSD13A gene. Published research associates it with allergic disease (asthma, hay fever or eczema). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs10883723 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 rs10883723 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 rs10883723 come from?

GWAS Catalog, Human molecular genetics 2019, PMID:31361310. 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.

Allergic disease (asthma, hay fever or eczema) (rs10883723). MyGeneLog™. https://www.mygenelog.com/variants/rs10883723

← See all variants