Standard

CD11c on myeloid Dendritic Cell

ITGAM · rs188316112

What the study found

Who was studied 2,872 Sardinian (founder/genetic isolate) ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.941 lower (95% confidence interval 0.64-1.24); p = 2 × 10−9.

How common The A allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 16, band 16p11.2 — in an intron of ITGAM.

What each result means

A/A Two copies of the version the research linked to CD11c on myeloid Dendritic Cell. 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 CD11c on myeloid Dendritic Cell. That is a smaller link than two copies.
G/G No copy of the version the research linked to CD11c on myeloid Dendritic Cell. This is the starting point the study compared everyone against.
Source

Questions about rs188316112

What is rs188316112?

rs188316112 is a single position in the genome, in or near the ITGAM gene. Published research associates it with cd11c on myeloid dendritic cell. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs188316112 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 rs188316112 come from?

GWAS Catalog, Nature genetics 2020, PMID:32929287. 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.

CD11c on myeloid Dendritic Cell (rs188316112). MyGeneLog™. https://www.mygenelog.com/variants/rs188316112

← See all variants