I’m not sure I can answer that question, but I can tell you that I am a total gene-holic, and I think it is important to know what genes are and what they do, because, if you know about what genes are, you can make your own decisions about whether to use them.
Genes are the genes from one parent passed on to the next, and they are very important for life. But what they do can be a little confusing. What they do is they make your DNA code unique to you. Because of this, different people have different amounts of genetic material that is passed from one generation to the next. It is this unique genetic material that you are born with, and it is this unique genetic material that you will inherit from your parents.
The whole concept of this genetic material is called “genome.” You can think of it as a very large DNA file, and it is actually stored and passed down from generation to generation. As a result, a single human has hundreds of different versions of the same gene, and all of these are present in the person you are born into. It can be said that the individual’s “genome” is the sum total of their DNA.
The thing is that not all people that have the same genome are exactly the same, which means that it can be very confusing for the person to understand what each of their particular gene variants mean. This is why the term “genome wide association” was invented to describe this kind of individual variation.
This is where the gene variant comparison becomes helpful. We can say that a gene variant is present in a population because that particular variant has been tested in one or more individuals with that specific gene. The way that this works is that we test a person, and if they have that particular variant that we’ve tested, then we can say that they are exposed to the specific variant.
The way we can say that somebody is exposed to a gene variant is by having them genetically tested. So if we test people against each other, it’s possible to compare the genetic differences between individuals to see if there are any similarities or differences.
It’s a little more complicated than that. The DNA sample is typically taken from a person’s blood, so we can test for many genes, and if we find that the person has one of the variant genes we tested, we can say that they are exposed to that variant. Of course, most people who have this variant don’t have it, so there is a pretty good chance that they are not exposed to that variant (i.e. they have a different variant of the gene).
I find it pretty funny that most people dont seem to know what the word “variant” means, because they think that it means something completely different than it means. There are many different types of variants, and one of the more common kinds is called a “polymorphism.” Variants are the little variations that make up a person’s unique DNA code, and they are different than the standard version of DNA that everyone has.
Polymorphisms are genetic variants that exist, but not in the standard code. Polymorphisms occur in people who have a rare variant of a gene, or are more than one variant from the standard code. Polymorphisms are usually only one variant of that gene, but can be two or more separate variants. This is very important to know because it’s the only way that you can actually determine whether a person has a rare gene or two separate genes that are different than the standard code.
Polymorphisms are very rare, so the question is how rare they are. For the sake of this article, I’ll assume you want to know that a certain gene is the only genetic variant in a population.