TTR-related hereditary amyloidosis is often managed by treating the symptoms through medications or surgical intervention. However, some recently approved medications work by decreasing the production of the TTR protein, which makes it less likely to build up in the body's tissues and organs. In addition, most of the TTR protein is produced in the liver, and liver transplants have been beneficial for some patients. Scientists are currently working on other treatment options for this condition.
Bill Newman, professor of translational genomic medicine in the Manchester centre for genomic medicine at the University of Manchester, and chair of the British Society of Genetic Medicine, says that such tests in this context simply don’t make sense and that, usually, telomere testing would only be used in in-depth studies of ageing and diseases associated with ageing. “There’s some really brilliant work going on, by some of the best biologists in the world,” says Newman, citing Elizabeth Blackburn, who won the 2009 Nobel prize for medicine for her work on telomeres. “But there’s no evidence whatsoever that measuring a person’s telomeres gives any indication about their health – or beauty, intelligence, or anything else that might be listed on these sites.”
Some concerns about the ultimate efficacy of certain home tests seem to emanate from the industry itself. I did a telomere-measuring test (a mouth swab) by Titanovo, based in north Colorado, which came back saying that my telomeres were too short, putting me at 10 biological years older than I am. However, when I contacted Titanovo, it explained that it had stopped telomere measuring and was now concentrating exclusively on its DNA-utilising “bioinformatics” health, fitness and wellbeing website (analysing client data from other genetic testing sites).
Of the 23 pairs of chromosomes in the human genome, 22 are autosomes. Most direct-to-consumer DNA tests look primarily at your autosomal DNA to determine your geographic ancestry percentages. This DNA is a mix of inherited DNA segments – half from each parent. Because everyone inherits at least one X chromosome from their mother, DNA tests often include the X chromosome in autosomal testing, though the X chromosome is not an autosome.
G6PD deficiency is a common genetic condition caused by defects in an enzyme called glucose-6-phosphate dehydrogenase, or G6PD. The G6PD enzyme helps protect red blood cells from damage. In people with G6PD deficiency, red blood cells are destroyed upon exposure to certain environmental triggers, which can lead to episodes of anemia. This test includes the most common variant linked to G6PD deficiency in people of African descent.
I have had my DNA done at ancestry.com & 23&me, ancestry.com & 23 are basically the same until it gets to the trace regions… ancestry says I am 1% Euro Jew which made since with my haplogroup K1a3a, but 23andme gave me .08% African, changed date when it occurred 2x went from East to West, then settled on “Sub African”, none of which I believe occurred due to my own research but if in fact I am either Euro Jew,(I think it is non-mixed Israelite/Hebrew, but whatever), and or if their is this .08 African, I’d like to know why ancestry did pick up on it, how sure they are at 23&me,(they can’t tell Irish from Brits or German from French but can go on & on about some supposed .08% makes no sense), BUT now that it has been said, I want to put it to rest… If either occurred can I confirm using the raw DNA I have from both? Shouldn’t both be able to say I am or am not Jew or African? I don’t care either way, but want to know what site would be able to answer this the best…. again I have raw data/dna from both ancestry.com & 23 & me. HELP 🙂 Thank you in advance.
DNA profiling can be useful in determining whether a person was present at a crime. If a DNA profile obtained from a scene sample matches that of a suspect, that DNA could have come from the suspect or from someone else who happens, by chance, to have the same DNA profile. However, not all DNA profiles carry the same evidential value. Some may provide extremely strong evidence of association while others may be of poor quality and of limited evidential value.