$49 Personal Genome at 23andme (incognito windows until you get the best price)
23andme.com
23andme.com
document.cookie = 'optimizelyBuckets=' + escape('{"145285685":"145865258"}') + '; domain=.23andme.com'; document.location.reload(true);
The other values I found: 69 -> escape('{"145285685":"145818631"}')
99 -> escape('{"145285685":"145866265"}')
149 -> escape('{"145285685":"145285686"}')
299 -> escape('{"145285685":"145891045"}')
Edit: Actually, it looks like this no longer works. They may have noticed and stopped the A/B test.You can empty the cart and run
window.$.ajax({url:'/special_offer/49NOV2012/?json=true'})
Then click add to cart and once in your cart it will be $49.I'm going to have to start looking at more websites' Optimizely codes!
Anyone else having any luck?
What I want to know is, who they share the data with? Do the insurance companies get our genome?
Come on people, there should be no more precious data to you, than the genome of you and your family. Yet facebook users seem more concerned about their social network privacy than HN members are about their genome privacy.
For insurance companies, this could be a total actuarial GOLDMINE and it would probably even be worth them paying us for the data.
Also, quite a few people have been posting their data openly, for example here: http://opensnp.org/ . So far I am not aware of any adverse effects. Not saying there won't be any ever, but I would be a lot more paranoid about my browser history.
Did you read the privacy policy? Specifically:
https://customercare.23andme.com/entries/21262376-how-is-the...
23andMe research may involve collaboration with external parties; however, these external parties will only have access to pooled data stripped of identifying information. 23andMe will never release your individual-level data to any third party without asking for and receiving your explicit authorization to do so. As part of our commitment to protecting the privacy of our research participants, we have also obtained a Certificate of Confidentiality from the U.S. Department of Health and Human Services. This certificate allows 23andMe to protect research participants’ data from involuntary disclosure, including subpoenas from federal, state, and local authorities.
>Do the insurance companies get our genome?
They're not allowed to discriminate based on genetic predisposition, and based on the privacy policy, they're not going to get that info anyways.
https://www.23andme.com/about/privacy/#Full
It's pretty clear on what they choose to share.
It is nice that their website includes reassuring language. But really, how stable is that policy in the face of changing corporate owners, changing political administration (romney?), changing supreme court justices, changing geopolitics?
Genome data is of permanent importance. To be able to, even in 50 years, look back at genome records of today, will still be very valuable (especially when combined with genealogy records...).
Look at privacy trends, storage trends, and trends in govt accountability and transparency. Make no mistake, once our sequences are in corporate databases, there is no going back.
I look forward to user-driven cryptographic genome tools, which will allow us to inspect our own genomes, while maintaining personal control over our entire genome (ie., never having to hand the whole sequence over to a commercial or govt entity).
That's a valid point, but a few things reassure me. Firstly that confidentiality cert from DHHS probably isn't going to be made useless by a political entity any time soon (and I'd assume, though would need to research, that such a cert would also apply to any buyers should 23AM get picked up by someone else, and probably carries some requirements for them as well)
Even then, I doubt within the next 60 or so years left on my lifespan that there will be any shenanigans in that area... and after I'm gone, they can do whatever the hell they want with my sequence :)
I'd imagine that, given enough time and cost reduction, services like this will become nationalized, where your genome is sequenced at birth for identity and health purposes.
And as for insurance, I think that applies in the US where insurance companies are, well, evil. In AU, or CAN or some other country where medicine is provided to everyone, this actually seems like GOOD information to have on hand.
In the long-term, it's unlikely that you'll be able hide your genome. Sequencing technology is only going to get cheaper and more advanced. People slough off cells like crazy. You'll have to live in a spacesuit if you want to avoid leaving your genetic information everywhere.
1. http://en.wikipedia.org/wiki/Genetic_Information_Nondiscrimi...
I had to keep closing and creating a new incognito window, not just new tabs.
It's cheaper to create a new account then to upgrade my old account for $249.
You get more SNPs if you have V2 and they add in V3, so I'll call them and see if I can link it to my account.
Here are the SNP counts per chip version combo:
V2 only: 576,000 SNPs V3 only: 967,000 SNPs V2 + V3 (upgraded): 996,000 SNPs
""" 23andMe is currently unable to process saliva samples collected in or mailed from the state of New York. The New York Department of Health considers our Personal Genome Service a test requiring a lab license and direct physician involvement.
If you or the recipient of the Spit Kit intend to collect your sample and mail it from outside the state of New York, please select the "Ship to New York" button below. Upon receipt of your Spit Kit, you or the Spit Kit recipient will be required to affirm under penalty of law that the sample for the Spit Kit has not been collected in or mailed from the state of New York."""
I use this:
https://chrome.google.com/webstore/detail/edit-this-cookie/f...
The value used to be that you get the newest research linked to your SNPs, i.e., if there's a new publication on one of your variations you would have been notified.
That said, hopefully they do some A/B testing on shipping prices next ;)
Right?
According to this NIH page on said certificates[2], it sounds like even if they were served a subpoena for the information, 23andme could still tell them to fuck off.
[1] https://customercare.23andme.com/entries/21262376-how-is-the...
It's certainly worth $49 to me to know this (I think I paid $99 under a FNF deal a while ago; I know one of the founders, who is awesome and a great entrepreneur).
The only real risk I see is if your account is compromised somehow, but at least for me, there's nothing so sensitive in my account that I'd care.
Edit: ftp://ftp.1000genomes.ebi.ac.uk/vol1/ftp/ <-- gimme this for $49
http://www.genomicslawreport.com/index.php/2012/11/29/dna-dt...
>Whole exomes ($695 at 80x coverage) and genomes ($5,495 at 30x coverage) are both listed as available products.
Got mine for $49. Note once you get $49, you can order multiple kits at that same price point.