this post was submitted on 19 Nov 2023
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Maybe a naive question, but Is there a service like 23 and me but that doesn’t collect/keep my genetic information ? @[email protected]

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[–] [email protected] 51 points 2 years ago (2 children)

It’s absolutely abusive that in order to get your genetic background you have to be willing for the government to have your DNA.

[–] [email protected] 13 points 2 years ago (1 children)

It's not even gouvernement, it's other companies. One day some insurance company will decide to pull out your protections because, turns out, you have X% chances to get a cancer by your 40. Then all other insurance companies do the same. Then, one of them accepts you, but you gotta pay N% more for the same coverage

[–] [email protected] 4 points 2 years ago

That’s the fear. Government was just used as hyperbole to make a point.

[–] [email protected] 26 points 2 years ago

No. Every DNA collecting agent in the U.S. easily shares it's data base.

[–] [email protected] 22 points 2 years ago* (last edited 2 years ago) (1 children)

I've been wondering this myself. I don't really agree with the other comments saying it's impossible.

We do genetic testing on the medical side and that data is kept private. I don't see why a company couldn't offer similar stuff, paid privately, for a more comprehensive suite of tests. You could learn about your risk factors and keep the data private.

On the history/ancestry side, it could pick out known biomarkers to trace back from publicly accessible data. You wouldn't be able to track down exact family trees, but I don't think that was the intent since you're looking for privacy. Instead you might get stuff like "you're 40% Greek, 20% North African"

Such a company would

  • collect a sample
  • compare the data against literature
  • delete the data

It could also allow customers to opt in for more detailed analysis (for those that don't care for privacy) and let them know about the risks. Or it could give an option to share anonymized health data for researchers investigating diseases / risk factors

Edit: see the comment by [email protected]

[–] [email protected] 16 points 2 years ago (1 children)

Nope. And everyone knew what 23 and Me was doing and did it anyway.

[–] [email protected] 6 points 2 years ago* (last edited 2 years ago)

Is there a reason one can't exist? Like laws that prevent them from doing so?

There's a lot of good that can come from genetic screening (ex. medical care), it would be a shame if we'd lose all that because of a dumb law

[–] [email protected] 11 points 2 years ago (1 children)

Not to my knowledge. It's absolutely pathetic and honestly kinda psychotic that you're not allowed to understand your own genealogy and medical history without giving up pretty much everything about yourself. Forever.

Because unlike a compromised password, you can't just hop on the computer and change your genes (yet??).

Boils down to a legislative failure.

[–] [email protected] 4 points 1 year ago (1 children)

Presenting swirlies: a fun fingerprint matching platform. Send in your fingerprints and get to know your fingerprint relatives. Swirls, loops and curves - we got it all! Find new soulmates at swirlies, only 15$ per analysis and 2.99$/year to access the app and keep up to date with your fellow swirlies.

[–] [email protected] 5 points 1 year ago

When I was in like 5th grade we took a class trip to a police station.

Once we got there the cops said if we were "good" he'd let us do fingerprints at the end. I was excited till I found out we didn't get to keep the cards, the cops did and they said it was in case we get kidnapped they can find us... When a minute ago it was just a reward for being good.

So I said I didn't want to and the cop and teacher got super pushy and it turned into this whole big thing once parents found out every kid from my school for a couple years got tricked into giving cops their fingerprints.

I was just mad I didn't get to keep the card, they should've just had me do two and kept one.

[–] [email protected] 8 points 2 years ago (1 children)

Is there any benefit for those kinds of services. Other than just for fun, I don't see any reason for it.

[–] [email protected] 2 points 2 years ago

Having access to diseases that run in your family when you are adopted is a great benefit of it, and doing that at a private lab is way more expensive. And the one my sister did connected her with family members who were interested in being contacted. It's not that there is a lack of benefit to the service, it's that the services aren't worth the privacy intrusion.

[–] [email protected] 8 points 1 year ago* (last edited 1 year ago)

Recently I listened to a Crime Junkie episode where they recommended you send your DNA in for genetic genealogy so that if a John Doe or Jane Doe turns up they can be identified and I was like lmfao no thanks why would I do that when I know they're gonna send it everywhere, to advertisers, to law enforcement,... and I have no way of controlling it. People really don't give a fuck about their privacy. Honestly, it boggles me.

[–] [email protected] 5 points 1 year ago (1 children)

The problem is that to be able to tell you anything about relationships or heritage, they need a certain database, and the quality of that depends on the amount of entries to compare.

Without adding your data set to the collection, they would not gain anything to improve their database, which would de-value it in the long run.

A service that would analyse but not retain your data would have to pay other companies to provide input, and would therefore much more expensive.

[–] [email protected] 3 points 1 year ago (2 children)

@[email protected] That's fine, but I'm more interested in the genertic markers that can be associated to diseases more than finding my ancestry tbh

[–] [email protected] 2 points 1 year ago

Still, those reasons apply. If you want such a service, expect to pay way more than usual. I do expect that some companies offer such a service for VIPs and Celebrities who don't want to pop up in other peoples listings, but they probably pay for it through the nose.

[–] [email protected] 1 points 1 year ago

Are you sure you cannot simply opt out while registering the sample? I live in Germany and I can only use these kinds of analyses for ethnicity/heritage analysis since genetic testing of risk factors as therelike are forbidden here. But I remember myheritage (which I used) asked me a lot of questions on how much data I want to share, what I want to share anonymously, what I want to share for research or keep in the database or sample storage for future analyses. I was also able to absolutely delete all data - account, sample destruction, genetic data - from every database. Comes with the obvious caveat that you cannot access any data from your initial analysis anymore but in my situation that was an ok trade off.

[–] [email protected] 2 points 2 years ago (2 children)

Seems to me the hard part is getting the customers to pay the "full" price of getting the genetic sequencing done. 23andme's prices to get tested is rather expensive (> $130 the last time I checked) but they are also getting paid for providing some of that data for various "studies". So they are getting paid to collect and keep the genetic data, so the consumer price of testing ($130) is subsidized by the other revenue channel (i.e. selling access to the data).

I don't know how much it costs to get your genes sequenced, but it's probably more than $130 per sample.

I see it like ads.... as much as everyone wants to complain about watching ads, the alternative is to pay the full price for the service you are consuming. Most of the services we consume are - after all - profit-making companies, and even the ones that aren't have bills that need paying.

[–] [email protected] 1 points 2 years ago (1 children)

@[email protected] the difference is that you can’t change your genetic information. It is more like your SSN.

[–] [email protected] 1 points 2 years ago
[–] [email protected] 1 points 2 years ago

If we could pick and choose what we share then it might not be so bad, but commodification of genetic information is weird.