DasFX. I don't call you a racist, because I see no evidence that your misperceptions are based in racism. But you are wrong about race.
It has no biological meaning, only a social one.
You say you're in pharmaceutical research, designing a drug that is race-specific. I say nonsense. I know I can find at leat one other "racial" group who will respond in general like your target "race" to whatever drug you're trying to create. There are so many so-called "race-specific" genes whose specificity is BS. The mutant hemaglobin gene responsible for the condition of sickle-cell anemia is present in different forms in geographically separate populations, in West Africa, Sicily and India, suggesting that the predominant forms of the mutation arose independently among these diverse populations. The selective pressure for this mutation is the incidence of malaria in these regions and the resistance the mishapen red blood cells give to the inheritor of the mutant gnenes. "Race" has nothing to do with it.
Here is the state of the science:
Quotes are from R.C. Lewontin's article at this site, which is probably the most authoritative website on "race" and genomics.
It has no biological meaning, only a social one.
You say you're in pharmaceutical research, designing a drug that is race-specific. I say nonsense. I know I can find at leat one other "racial" group who will respond in general like your target "race" to whatever drug you're trying to create. There are so many so-called "race-specific" genes whose specificity is BS. The mutant hemaglobin gene responsible for the condition of sickle-cell anemia is present in different forms in geographically separate populations, in West Africa, Sicily and India, suggesting that the predominant forms of the mutation arose independently among these diverse populations. The selective pressure for this mutation is the incidence of malaria in these regions and the resistance the mishapen red blood cells give to the inheritor of the mutant gnenes. "Race" has nothing to do with it.
Here is the state of the science:
Over the last thirty five years a major change has taken place in our biological understanding of the concept of human “race,” largely as a consequence of an immense increase in our knowledge of human genetics. As a biological rather than a social construct, “race” has ceased to be seen as a fundamental reality characterizing the human species. Nevertheless, there appear from time to time claims that racial categories represent not arbitrary socially and historically defined groups but objective biological divisions based on genetic differences.
There are four facts about human variation upon which there is universal agreement. First, the human species as a whole has immense genetic variation from individual to individual. Any two unrelated human beings differ by about 3 million distinct DNA variants.
Second, by far the largest amount of that variation, about 85%, is among individuals within local national or linguistic populations, within the French, within the Kikuyu, within the Japanese. There is diversity from population to population in how much genetic variation each contains, depending upon how much immigration into the population has occurred from a variety of other groups and also on the size of the population
Of the remaining 15% of human variation, between a quarter and a half is between local populations within classically defined human “races,” between the French and the Ukrainians, between the Kikuyu and the Ewe, between the Japanese and the Koreans. The remaining variation, about 6% to 10% of the total human variation is between the classically defined geographical races that we think of in an everyday sense as identified by skin color, hair form, and nose shape.
Third, a small number of genetic traits, such as skin color, hair form, nose shape (traits for which the genes have not actually been identified) and a relatively few proteins like the Rh blood type, vary together so that many populations with very dark skin color will also have dark tightly curled hair, broad noses and a high frequency of the Rh blood type R0. Those who, like Leroi, argue for the objective reality of racial divisions claim that when such covariation is taken into account, clear-cut racial divisions will appear and that these divisions will correspond largely to the classical division of the world into Whites, Blacks, Yellows, Reds and Browns. It is indeed possible to combine the information from covarying traits into weighted averages that take account of the traits' covariation (technically known as "principal components" of variation). When this has been done, however, the results have not borne out the claims for racial divisions. The geographical maps of principal component values constructed by Cavalli, Menozzi and Piazza in their famous The History and Geography of Human Genes show continuous variation over the whole world with no sharp boundaries and with no greater similarity occurring between Western and Eastern Europeans than between Europeans and Africans! Thus, the classically defined races do not appear from an unprejudiced description of human variation.
The fourth and last fact about genetic differences between groups is that these differences are in the process of breaking down because of the very large amount of migration and intergroup mating that was always true episodically in the history of the human species but is now more widespread than ever. The result is that individuals identified by themselves or others as belonging to one “race,” based on the small number of visible characters used in classical race definitions, are likely to have ancestry that is a mixture of these groups, a fact that has considerable significance for the medical uses of race identification.
Quotes are from R.C. Lewontin's article at this site, which is probably the most authoritative website on "race" and genomics.