Sequencings

Markers / IL6R

rs2228145

The interleukin-6 receptor, and a drug target found by genetics

GeneIL6R
Positionchr1:154,426,970
VersionsA / C
Evidenceestablished

What this position does

IL-6 is a central inflammation signal. This variant shifts receptors off cell surfaces into the blood, which dampens the signal, and carriers have a slightly lower risk of coronary heart disease. That finding is a large part of why IL-6 blockade was pursued as a heart drug at all.

Immune system. Shaped by inflammation, useful acutely and harmful chronically. This is one of the variants that differs sharply between human populations, because something in the environment made one version worth having.

Infection, and the cost of fighting it

For most of human history the commonest way to die young was infection. An immune system tuned to win those fights is tuned for a world that, in rich countries, no longer exists.

What changed: Industry, roughly the last two centuries. Indoor work, heated buildings, refined food, cheap salt and sugar, tobacco at scale, and a collapse in infectious disease. This is where most of the deals in your genome came undone.

Why it spread: nobody knows. The frequency difference between populations is real and measured. What the variant was worth having for is not known, and any site that tells you is guessing.

Spiral Staircase, chapter 20: The Fever and the Old Enemies Spiral Staircase is written by the same author as this site.

What each result means

If you carryWhat it means
No copies of the effect version
AA
You have the common version on both copies
Standard IL-6 receptor signalling.
One copy
AC
You carry one copy
Associated with slightly dampened IL-6 signalling and a modestly lower risk of coronary heart disease.
Two copies
CC
You carry two copies
The strongest form of the same small effect, and a slightly higher C-reactive protein reading, which is a measurement artefact of the receptor shift rather than more inflammation.

How common each version is

Ancestry groupC (the effect version)
African8.7%
American53.6%
East Asian32.3%
European36.0%
South Asian30.0%

1000 Genomes Project phase 3, via Ensembl, retrieved 2026-09-23. These groupings are coarse and flatten a great deal of internal diversity, particularly within Africa. A variant being common somewhere tells you where a piece of your ancestry probably comes from, and nothing else.

How many people carry each result

Ancestry groupAAACCC
African551 / 661105 / 6615 / 661
European208 / 503228 / 50367 / 503
East Asian231 / 504220 / 50453 / 504
South Asian237 / 489211 / 48941 / 489
American74 / 347174 / 34799 / 347

Counts of people, not modelled frequencies: every one of the 2,504 individuals sequenced by the 1000 Genomes Project phase 3, tallied by the genotype they carry. Deriving these from allele frequencies instead would assume random mating inside each group and undercount the homozygotes.

How to find out which you have

If you have taken a test with 23andMe, AncestryDNA, MyHeritage, Family Tree DNA, TellMeGen or Living DNA, this position is very likely already in the raw data file they gave you. You do not need another test.

One thing to watch if you look it up by hand: testing companies report some positions from one DNA strand and some from the other, and the file does not say which. Read the letters as they appear and you will get the opposite of the truth for some positions. Sequencings resolves that automatically.

Source

IL6R Genetics Consortium, Interleukin-6 receptor pathways in coronary heart disease, The Lancet (2012)

Coordinates and allele pair verified against Ensembl GRCh37. Direction of effect verified against VEP protein consequences or 1000 Genomes population frequency. Category: Population adaptation.

Where this fits

Common questions

What is rs2228145?

rs2228145 is a position in the IL6R gene on chromosome 1. IL-6 is a central inflammation signal. This variant shifts receptors off cell surfaces into the blood, which dampens the signal, and carriers have a slightly lower risk of coronary heart disease. That finding is a large part of why IL-6 blockade was pursued as a heart drug at all.

What does it mean if I have CC at rs2228145?

You carry two copies. The strongest form of the same small effect, and a slightly higher C-reactive protein reading, which is a measurement artefact of the receptor shift rather than more inflammation.

What does it mean if I have AA at rs2228145?

You have the common version on both copies. Standard IL-6 receptor signalling.

How do I find out my rs2228145 genotype?

If you have taken a home DNA test, this position is very likely in the raw data file you were given. Sequencings reads that file in your browser without uploading it, and resolves which DNA strand each position was reported from, which is the step most manual lookups get wrong.

This is reference information, not medical advice, and not a diagnosis. See the medical disclaimer. Category: Population adaptation.