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PDL-1 on monocyte

FCGR2A · rs9427401

What the study found

Who was studied 3,629 Sardinian (founder/genetic isolate) ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.273 lower (95% confidence interval 0.22-0.33); p = 2 × 10−20.

How common The G allele had a frequency of about 23% in the people studied.

Where it sits Chromosome 1, band 1q23.3 — in an intron of FCGR2A.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of PDL-1 on monocyte — no copies of the reported risk allele.
C/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with PDL-1 on monocyte.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of PDL-1 on monocyte compared to the general population.
Source

Questions about rs9427401

What is rs9427401?

rs9427401 is a single position in the genome, in or near the FCGR2A gene. Published research associates it with pdl-1 on monocyte. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs9427401 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 rs9427401 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

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PDL-1 on monocyte (rs9427401). MyGeneLog™. https://www.mygenelog.com/variants/rs9427401

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