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THE DNA TEST THAT FOOLED AND SILENCED AMERICAN AFROCENTRICS
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[QUOTE]Originally posted by Baalberith: [QB] [QUOTE]Originally posted by Baalberith: [qb] [QUOTE]Originally posted by Ase: [qb] No, limb proportions are supposed to help infer genetic relationship and proximity. But if people that are say Adamanese can be Black but are gentically closer to Asians than Africans there is no "genetic" relationship that grounds race. Never stated race was anything but a socially constructed argument, but I see your point. I don't want to teach or insist on people to accept irrelevant data to race. I don't subscribe to race being a valid genetic construct, therefore I feel it is important to not be selective in when I express that point of view. Alright, fair enough. [QUOTE]Also, you state that Lower Egyptian's crania was similar to European populations than Ethiopians, via phenotype, again given how situated the Levant and better yet Lower Egypt is geographically in a arid environment, while there Southerner counterparts at in a tropical environment, how exactly does them having similar crania like Europeans, as some former 19th century and 20th century Egyptologists have claimed, alright so be it. But still given the fact that various Mesolithic Middle Easterner and even African populations were and are phenotypically distinct from one another I still fail to see your position on Lower Egyptians's and Levantine "intermixture". [/QUOTE]I'm confused, If memory serves the origin of light skin found in Europeans came from a common ancestor that originated between the Indian sub continent and the Middle East. [QUOTE]Abstract Divergent natural selection caused by differences in solar exposure has resulted in distinctive variations in skin color between human populations. The derived light skin color allele of the SLC24A5 gene, A111T, predominates in populations of Western Eurasian ancestry. To gain insight into when and where this mutation arose, we defined common haplotypes in the genomic region around SLC24A5 across diverse human populations and deduced phylogenetic relationships between them. Virtually all chromosomes carrying the A111T allele share a single 78-kb haplotype that we call C11, indicating that all instances of this mutation in human populations share a common origin. The C11 haplotype was most likely created by a crossover between two haplotypes, followed by the A111T mutation. The two parental precursor haplotypes are found from East Asia to the Americas but are nearly absent in Africa. The distributions of C11 and its parental haplotypes make it most likely[b]that these two last steps occurred between the Middle East and the Indian subcontinent, with the A111T mutation occurring after the split between the ancestors of Europeans and East Asians.[/b][/QUOTE] https://www.g3journal.org/content/3/11/2059.abstract [/qb] Interesting stuff, I real check this out. [/QB][/QUOTE]
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