>>51738418>>51738424There are one base pair mutations in genetic code that can be identified by sequencing. These SNPs, once you find them, may correspond to a certain gene, which then has to be identified. These gene designations corresponding to the SNPs are given below:
5p13, 5q31, 7q32, 8p22, and 10q23
These genes code for protein subunits of glutamate membrane transport proteins.
For the Xq28 type of homosexuality, there is a distinct facial phenotype in dual expression. The Xq28 gene is part of the melanoma associated antigen family of genes that’s involved in surveillance against melanoma cancer.
The Xq28 gene is related to diseases of extreme ‘maleness’ like autism, ADHD, asperger syndrome, etc. The Xq28 gene, if doubly expressed in males, creates an extreme phenotype. The child is severely autistic, has ADHD, is homosexual with gender nonconformity, and has an extreme version of the le /pol/ face. In normal single expression, variations in gene product due to neonatal problems will still contribute to clinically significant phenotypes. Many incels are incels for the same reason some gays are gay.
https://en.wikipedia.org/wiki/Xq28 