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by aroch
330 days ago
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> However–and here’s the rub–some 25 years after the human genome was sequenced, and despite huge efforts to link genes and disease, there are almost no SNPs that tell you anything consequential about your health. If you have a genetic disease, you almost certainly already know about it, and if you don’t know, then the 23andMe data just isn’t going to reveal anything. For someone who “knows genomes”, this is a brain dead take on microarrays. Lots of the content on arrays _is_ directly tied to a phenotype because there’s limited space so we directly test variants that are known to cause problems! Is he really claiming that BRCA1/2 variants don’t increase risk of breast cancer in a meaningful way? Or that there aren’t tons of people who are XXY who don’t know even though it’s the hidden cause of many infertility problems? This is just such a bad take it is hard to take anything said here seriously |
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Even worse, if insurance companies had their way, they'd use the family matriarch's BRCA1/2 variant to set the rates for all her descendants. Massive DNA profiling doesn't just impact the "owner" of the DNA - it impacts anybody in their family tree who might have similar genes.