Recent Updates
7/21/2017
Significant Upgrade to %'s and Bar Graph in our Reports
Our previous reports showed a percentage at the end of the enzyme listing that simply indicated what % of the genes were not a genetic variant. Although this was helpful, it also created some confusion in its interpretation because SNPs not variated does not reflect the actual function.
The color still remains. This color reflects how your patient/client compares to the average, or mean of the entire data base. The more green the color, the better they are than the mean, and the more yellow and red, the more SNPs they have compared to the mean
.
When you click on the bar chart, located to the right of the color block, you will notice it now has a bell curve. We will be making a video to explain this in the near future.
To make it even more effective, we are working on a rating of -5 to 5 that will reflect how far they are from the mean. This will be much more meaningful data.
And finally, the launch of the Pyramid will be very soon, where you can see at a glance, where support is needed. More information coming soon!
6/9/2017
MGNA SNP CHANGE UPDATE
There have been some changes in how the risk allele is being reported for TCN2 C766G rs1801198
If you look at various sites on the web, many of them have differing values for the risk. After conducting further research on this SNP, we have decided to use the 1000 genome projects population data to report the risk allele.
Be sure to check here for the messages about updates.
Thank for your use of the MGNA software. Our goal is to always be on the cutting edge!
5/12/2017
MGNA SNP CHANGE UPDATE
There have been some changes in how the risk allele is being reported for the CYP Genes.
If you look at various sites on the web, many of them have differing values for the risk. After conducting further research on the CYP SNPs included in the Practitioner Report, we have decided to use the 1000 genome projects population data to report the risk allele.
Be sure to check here for the messages about updates.
Thank for your use of the MGNA software. Our goal is to always be on the cutting edge!
4/17/2017
MGNA SNP CHANGE UPDATE
There have been some changes in how the risk allele is being reported for the Nrf2 Practitioner Report
If you look at various sites on the web, many of them have differing values for the risk. After conducting further research on the SNPs included in the Nrf2 Practitioner Report, we have decided to use the 1000 genome projects population data to report the risk allele.
Be sure to check here for the messages about updates.
Thank for your use of the MGNA software. Our goal is to always be on the cutting edge!
4/5/2017
MGNA SNP CHANGE UPDATE
There have been some changes in how the risk allele is being reported for CYP3A4*1B rs2740574
If you look at various sites on the web, many of them have differing values for the risk. After conducting further research on this SNP, we have decided to use the 1000 genome projects population data to report the risk allele.
Be sure to check here for the messages about updates.
Thank for your use of the MGNA software. Our goal is to always be on the cutting edge!
3/31/2017
MGNA SNP CHANGE UPDATE
There have been some changes in how some of the risk alleles are being reported for the Electron Transport Chain Complex 1-5 SNPs.
If you look at various sites on the web, many of them have differing values for the risk. After conducting further research on these SNPs, we have decided to use population data to report the risk allele.
Be sure to check here for the messages about updates.
Thank for your use of the MGNA software. Our goal is to always be on the cutting edge!
3/30/2017
MGNA UPDATE
You now have the ability to view the Lyme Study Practitioner report as a separate SNP report!
To view the Lyme Study Practitioner Report, click on the actions button next to the name of the client who you want to view the Lyme Study Practitioner report for.
Next, from the drop down to the right of Report select “Lyme Study Practitioner Report”
2/28/2017
MGNA SNP CHANGE UPDATE
There have been some changes in how the risk allele is being reported for KEAP1 rs11085735.
If you look at various sites on the web, many of them have differing values for the risk. After conducting further research on this SNP, we have decided to use the 1000 Genome Project Phase 3 population data to report the risk allele.
Be sure to check here for the messages about updates.
Thank for your use of the MGNA software. Our goal is to always be on the cutting edge!
12/27/2016
Symptom Survey Updates
-Upon receiving their symptom survey email, your clients will have ONE WEEK to start and complete the survey before the survey link expires.
-Please make sure your clients fill out their surveys on either a desktop computer or a laptop, and that they use Google Chrome.
11/28/2016
MGNA TRAINING CLASSES - MARK YOUR CALENDARS!
Please note changes to the Philadelphia dates.
Thank you everyone for your inquiry regarding our upcoming MethylGenetic Nutrition AnalysisTM training classes. The following dates are in the calendar for 2017.
MARCH 25 & 26 we will be in Philadelphia, PA
JULY 29 & 30 we will be in San Diego, CA
SEPT 30 - OCT 1 we will be in Chicago, IL
We have chosen these dates and locations for the MGNA Trainings for the East and West Coast and for Mid State for 2017. We will be sending out flyers, emails, and we will post on our www.methylgeneticnutritionclasses.com website more information regarding the cost and hotels.
For more information or to register, please call PHP/Nutritional Specialties at 1-800-245-1313 or for International calls 412-821-0388.
We look forward to having you there!
10/4/2016
MGNA SNP CHANGE UPDATE
There have been some changes in how the risk alleles are being reported for the AHCY and GRHPR genes.
If you look at various sites on the web, many of them have differing values for the risk. After conducting further research on these genes, we have decided to use the 1000 Genome Project Phase 3 population data to report the risk alleles for the AHCY and GRHPR genes.
Be sure to check here for the messages about updates.
Thank for your use of the MGNA software. Our goal is to always be on the cutting edge!
9/30/2016
Have any questions about the software?
Check out our new FAQ/Help section located next to the ‘Log Off’ button
From there you can find walkthrough videos on:
MGNA Basics
How to add a new Patient
How to set up Billing
How to send the Symptom Survey
And much more!
If you have any additional questions please contact Callie Zerby at
calliez@dnasupplementation.com
or call her at
717-733-2003 ext 312
6/4/2016
Many of you are asking why N/A sometimes comes up on a report. If someone has older 23andMe raw data, those older analysis' did not include some of the genes we are now analyzing. Also, occasionally 23andMe is not able to read the gene, and that will come up N/A, as well. Unfortunately, in these cases, the software is not able to do the calculations, and this is unavoidable. The best we can do as practitioners, is look at what is there, and make our best estimates of what is happening. However, if all the genes come up N/A then something did not upload properly. Please be certain you uploaded a zip file, and not a pdf of text file. Try uploading again, or contact us for technical support.
6/1/2016
IMPORTANT
Billing Changes - Due to your requests, positive feedback and all the exciting changes happening at DNASupplementation, we have implemented the following billing structure for your convenience.
Billing updates reflect the following:
$25.00 per month licensing fee ($300 per year) The licensing fee covers all updates on all your files and within the software, added SNP information, unlimited access to your files, educational videos and documents, and more.
$25.00 per patient (unlimited access) This is a one time cost per patient, there is no charge for re-entry into that patient's file to add lab numbers, symptoms survey uploads, etc.
Any previous subscriptions will be honored until the system prompts users to choose the new payment plan.
2/17/2016
MGNA SNP CHANGE UPDATE
Please click here http://conta.cc/1R6M5SG to learn more.
