With all due respect, I think you would benefit from some additional reading about how the world was populated.
It is not the case that there was sort of a central population which then migrated and diverged such that modern populations are all the terminus of spokes emanating from a central hub. In that kind of model, all modern populations are more or less equally diverse, more or less similarly related or unrelated, and more or less similarly clinal from one another. Another incorrect analogy might be the way leaves on a tree are all sort of equidistant from the trunk, and likely to be about equally related or unrelated to one another, since all the branches are sort of coming off the trunk the same way.
But that’s not what happened. Consider our mitrochondrial DNA lines. mtDNA is one way to trace ancestry. This has nothing to do with how much DNA is affected. It’s a way to trace antecedent groups.
If you start with mtDNA haplogroup L0 in africa, and get to the splitting off of L3 into M-N, you are roughly at the point of out of africa into the Levant, perhaps 50-70kya-ish. From there (broad picture; some exceptions for earlier exit groups yada yada) humans spread out to populate the world. Perhaps 30-40 kya the non-african ancestral group gets genes from a Neanderthal daddy. Other new variants appear (MCPH1 haplogroup D, e.g…that haplogroup happens to be named for Y chromosome markers, but doesn’t change the story). Out of africa, the gene variants that show up early in the Levant expansion (either ordinary evolution or archaic introgression) become an ancestral gene pool for the almost the entire out of africa group, and certainly most european and asian groups, who have M-N mtDNA lines as their ancestral group.
This is not the sub-saharan story. At L3/M-N, L3, L2 and L0 lines remain in africa, with all of the incredible diversity associated with those lines. But the gene variants which exist, and the new gene variants that arise, do so largely without exposure to out of africa gene variants post-Levant expansion.
That’s why I use that “M-N descendant lines” as shorthand, under the assumption that you are interested enough in the topic to get what I’m talking about.
To summarize: Most modern eurasians descended from the Levant population(s). Most modern sub-saharan africans descended from L0 without the Levant population being represented in their gene pool, because back flow did not occur on a large enough scale.
It’s easy to let wordsmithing around clinal populations, amount of SNP variations and so on mask the central concept here. When we self-identify into black, white and asian, we associate ourselves with very different average gene pools, on opposite sides of the out of africa splitting point.
Look at the diagram on page 614 here. The fat green lines are the main migrations and gene groups; the red crossbar lines show that there has been some gene flow between these large branches. Notice the splitting points, and the splitting point for europe, asia and the americas. Starting about 40kya, this is largely its own branch, with some backflow to NE africa in relatively modern times. Gene variants that arise among all of these branches flow mostly to descendant lines. A gene variant that arose in the Levant population 40 kya would flow to europe, asia and possibly the americas depending on the exact point where it arose. It might flow to NE africa. It would not be very represented for the rest of the african lines.
Notice also the language in the text: “sub-saharan populations…non-african populations…” You will see this language over and over again from population geneticists even when they take great pains to talk about quantity of diversity, no biology of race…etc etc.
Why do they use that language? Because “sub-saharan populations” and “non-african” populations are two different and diverged gene pools. And the modern populations they contain are nowhere near clinal with one another even though they may be clinal with their ancestral populations back to some original population (archaic introgression excepted for the M-M descendant lines).
This is why when we self-identify with “black,” “white” and “asian,” we self-identify with different gene pools even though there is no such thing as race and even though SNP variations run amok within all populations. And our migration history is the reason those self-identified genetic pools vary in average frequency for all sorts of gene variants.