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Popular Threads
- What "paperwork" should 23andme file?
- What "licences" should they obtain?
- Should people be allowed to order "non-medical tests" that can nonetheless reveal medical information, without going through a doctor?
- If a company wants to offer a cheap novelty product (eg: DNA, fingerprint, or blood tests), but doesn't want to run it's labs to medical / FBI / courtroom standards, what kind of legal disclaimer should it have?
- Why are the BRCA or statin tests necessarily "medical tests"? 23andme's position is basically: "These are tests for the curious. You cannot act medically on them. If you have health concerns, talk to your doctor and get yourself tested again by a real medical lab." Why is this not a legitimate position in your view?
http://www.thinkgene.com/if-somebody-came-to-yo...
The honest truth is that I'm still forming my opinions.
CLIA certification is a start, NYS and Ca State registration is a plus, ISO certification is even better.
Some states allow patients to order medical tests, some don't. Why not just call these few SNPs what they are, medical tests and let the law decide who orders what?
The disclaimer should read:" We are running a cheap knock off production and charging you entirely too much for it. In addition we are stealing your data and selling to the highest bidder. If you STILL want to use us rather than have your data safely protected from others looking to obtain your data...Heck, sign on up and join the conversation"
This is a clear move towards Clinical Applicability, stop fooling yourself.
-Steve
www.thegenesherpa.blogspot.com
My Casio says "not for use in diving", even though everyone knows it is waterproof to 100m. I use it when I snorkel. But when I dive, I pay extra for the SCUBA certified equipment. Should Casio be banned from making waterproof watches?
Your claim that 23andme is stealing data is (1) false, since their terms of consent are clearly spelled out; and (2) slanderous.
Your claim that they are charging too much is interesting. How much would YOU charge me to get the same tests and detailed background info I got from 23andme?
Face it: more people are interested in DTC companies' services than yours. Your attempt to use the government to prevent people from cheaply accessing their genetic data is unethical. YOU don't get to decide if I am allowed to access my OWN data.
I have never stated that 23andME should be represented by this disclaimer I suggested.
DNA retesting should not be prompted by whether the first test was cheap or not. It should be guided by how well do you trust the labs results. If the test results are not to be trusted, then even the public should not place their trust in them. Most tests are reliable.
As for your right to know your DNA......sure. But does a company have the ability to give you a clinical interpretation without accepting regulations THAT WE ALL HAVE TO ABIDE BY when we give clinical interpretation????
What is clinical interpretation? Descriptions which MAY be interpreted by the average person as able to be used for healthcare guidance. Plain and simple.
Have your As, Gs, Cs and Ts.......just skip the interpretation and my argument will be destroyed.
-Steve
www.thegenesherpa.blogspot.com