23andMe MJFF genetics 🧬 sub-study - Cure Parkinson's

Cure Parkinson's

25,479 members • 26,802 posts

23andMe MJFF genetics 🧬 sub-study

AmyLindy profile image
AmyLindy
•18 Replies

I submitted my sample 4 weeks ago. Excited & curious to see if Ancestry data comes back w the Genetics? What’s it like, anyone? Every 3 months we answer another round of questions, right?

Written by
AmyLindy profile image
AmyLindy
To view profiles and participate in discussions please or .
18 Replies
•

Someone from the study contacted me and scheduled an appt for a consultation to go over the results of my sample. It was a short call where they informed me I had no genetic markers for Parkinsons, in so far as what 23andMe tested. They went over any questions I had, asked if they could follow up w/me in the future, and that was about it. They seemed to be leaning more toward environmental causes or a mix of environment and genetics and listed head injury, pesticides, well water, insecticides and solvents as possible triggers.

PDGal4 profile image
PDGal4 in reply to

I had the exact same experience.

AmyLindy profile image
AmyLindy in reply to

Good to know!

Smittybear7 profile image
Smittybear7 in reply to

How do you get the test?

ddmagee1 profile image
ddmagee1

I had a good experience-no genetic markers for Parkinson’s; however, 23 and me came up with some very interesting facts about my descendants, and other ailments that I had genetic markers for. I general, it is a good thing to do, and it is frequently updated.

AmyLindy profile image
AmyLindy in reply to ddmagee1

Good !!!

MBAnderson profile image
MBAnderson

Amy,

I sent in my sample year ago and look at the data every few months. It's comprehensive. I never got a call, though. You must've filled out a survey on MJFF?

AmyLindy profile image
AmyLindy in reply to MBAnderson

Yes w questionnaire every 90 d I believe

Farooqji profile image
Farooqji

how much they charge for carrying out the tests

MBAnderson profile image
MBAnderson in reply to Farooqji

When I did it it was free for PWP.

Farooqji profile image
Farooqji in reply to MBAnderson

Can you please tell me their email address

Juliegrace profile image
Juliegrace in reply to Farooqji

Go to 23andme.com.

AmyLindy profile image
AmyLindy

Got my results last week! Fun stuff ;) and no PD markers.

SilentEchoes profile image
SilentEchoes

I was tested at the University of MN for Mendelian PD genes, also negative. The genetic counselor suggested whole exome sequencing. I did this with Genos before they required a prescription. This is medical grade testing. I then submitted my raw data file to Prometheus and Sequencing.com. You can do this with Ancestry.com and upload the VCF file to Prometheius. The is an inexpensive way to get WES information.

AmyLindy profile image
AmyLindy in reply to SilentEchoes

I used Prometheus, too!

AmyLindy profile image
AmyLindy

I don’t have anyone to interpret my deeper data, However. If there are any qualified volunteers, please advise?

SilentEchoes profile image
SilentEchoes

See if you can get a referral for genetic counseling.

AmyLindy profile image
AmyLindy in reply to SilentEchoes

I should do that- I’m worth it! (I sometimes feel like a pest...)

You may also like...

Major Breakthrough in Parkinson’s Research from MJFF

Genetic testing - nutrigenomics? Nutrahacker, Genetic genie, etc.

the data speak,\\" I finally decided to use data from a 23andme genetic test I'd taken years ago...

Genetic testing results

this is the case for 85% of people tested. I'm curious, have you been tested, and how many of you...

Ashkenazi Jewish Heritage: Genetics and Parkinson’s

but I didn't think to ask if they tested all genetic markers.

KARMET Study Begins Enrollment