Uh Oh
The system will not allow me to create an account (stuck on a little spinning circle). There is nothing wrong with my other apps. what gives?
Response from developer
Our system is working correctly. Please try again or contact us directly at the email address info@genomapp.com. Sorry for any inconvenience.
Great Presentation of Data
I really like how the data is presented in an easy to understand format. I sent it to my doctor and he is fascinated as well. I hope they include the marker/trait I am most curious about in their next database update.
Only as good as the data you give it
I uploaded my ancestry data to try to help understand some of the markers i have. Unfortunately i think Ancestry miscalls certain snps which likely confuses this app. It claimed i had vEDS and some 1 in a million disease that i obviously don't have. Cross check the data on open snp or snpedia before jumping to any conclusions.
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Android to iPhone switching
Purchases cannot be restored if you switch from Android to iPhone (or I imagine from iPhone to Android as well)
The info the app gives is good to know. I like the detail. Too bad I paid for full reports and can’t access them now. The “Help” section has an FAQ that doesn’t include this or how to contact their customer service.
The info the app gives is good to know. I like the detail. Too bad I paid for full reports and can’t access them now. The “Help” section has an FAQ that doesn’t include this or how to contact their customer service.
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Amazing App
This app is not for fun, it provides real reports based off your raw DNA. I recommend paying the small fee for the additional reports helped me diagnose an autoimmune disease. Easy to read and the information the app provides is plentiful!
Great app!
Very easy to navigate.
When will new version be out? Thank you!!
When will new version be out? Thank you!!
Response from developer
Thank you! We are working on it and we hope it will be ready soon!
Nice but the table of contents are at the bottom for the exported pdf!
Nice but the table of contents are at the bottom for the exported pdf!
Surveys
Why am I contributing all of my opinions and health for me to not get this information back. I can not subscribe to all services all the time. I just want some information from you if you want information from me.
Response from developer
First of all, please note that Genomapp does not access your DNA information, Genomapp is just a tool that allows you to compare your raw DNA data with scientific literature. Nor do we ask to contribute information. Besides that, Genomapp is not a subscription service.
No Update for 15 Months
The last database update was 15 months ago despite claims of an update interval of 6-12 months.
15 months of wait for update is too long.
I’m afraid the app is abandoned.
15 months of wait for update is too long.
I’m afraid the app is abandoned.
Love App but Please Update
I have loved and used the app for several years. It used to be updated regularly. It’s been a year, please update. 🙏🏼
Response from developer
Thanks for your support! We are currently working on a major update.
Run!!!
Did my ancestry before and wanted to use this app. It won’t upload my data from ancestry. I subscribed for the use, but can get access where to stop the continued subscription. This is bogus. I will need to block them from my Apple account.
Response from developer
Genomapp is not a subscription service. You must be referring to another app by mistake. If you need help transferring your file we would be glad to help. You can contact us at info@genomapp.com.
I’ve used Genomapp since 2015 and I love it!
The regular updates are great ! A few of the pathogenic results for complex diseases I had no signs of having in 2015. But since then I have developed 5 of the conditions I showed two copies of pathogenic markers. Three of those were familial breast cancer, neoplasm Of the breast, and cancer cell motility(the cancers ability to metastasize to other parts of the body. I have faithfully done my mammogram yearly ever since I got my first report. Feb 2,2021 I was diagnosed with invasive ductal carcinoma of the breast. I’ve since had surgery, I am cancer free, didn’t need radiation and only on anti hormone pills to prevent it from coming back somewhere else in my body. This app is partly responsible for saving my life as my cancer was caught early because I new my risks were high ! I used my ancestry dna file.the dna testing and Genomapp cost me less than $80! Most of that was the dna testing not Genomapp. I also love the links to Pubmed and National institute of health for learning, references, studies, and trials. I am a retired nurse.
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Unable to delete account
I can’t find where to delete my account
Approach with extreme caution.
This flagged BRCA 1 gene for me. A further more in depth test ruled thus out. The company who conducted the in-depth Breast Cancer Gene Panel for ne described the report generated by the Genomapp app as amongst the most poorly written and confusing they had ever seen.
The Genomapp report stated that I had two copies of a pathogenic variation in a point in the BRCA1 gene. The other genetic testing company informed me that two copies of a pathogenic gene at that point would mean I would have never developed fully as embryo, been carried to term and then been born. It’s basically impossible to have two copies and survive til birth. One copy of the variant would be considered pathogenic. As it turned out with further testing I had no pathogenic BRCA1 variants. This makes me think there are deficits in the construction and design of the reports and not just a mistake in the original test.
Update after developer response:
The developer has missed the point, It is medically impossible to survive until birth with two copies of that marker. So even if the error is in the data rather than the report, that should have been picked up as an error rather than merely flagged as a pathogenic marker. Hence the title “Approach with extreme caution”.
The Genomapp report stated that I had two copies of a pathogenic variation in a point in the BRCA1 gene. The other genetic testing company informed me that two copies of a pathogenic gene at that point would mean I would have never developed fully as embryo, been carried to term and then been born. It’s basically impossible to have two copies and survive til birth. One copy of the variant would be considered pathogenic. As it turned out with further testing I had no pathogenic BRCA1 variants. This makes me think there are deficits in the construction and design of the reports and not just a mistake in the original test.
Update after developer response:
The developer has missed the point, It is medically impossible to survive until birth with two copies of that marker. So even if the error is in the data rather than the report, that should have been picked up as an error rather than merely flagged as a pathogenic marker. Hence the title “Approach with extreme caution”.
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Absolutely awesome
Very in-depth
How to use this?
I can’t transfer any files to the app. I have last iPhone and not sure this app works well with Apple
Don’t jump to worse case scenario
Reviewing this information without proper psychological support can make you think you’re doomed due to genetics. Providing some level of genetic counseling would be something many of us would be interested in.
Not worth it
Will not process file. Only cycles to the dna provider type. Useless... inadequate FAQ and product support. Don’t store your data here. Better off using Other open source analyzers.
Lovethe app!
I have to let you know that I am thankful for the GenoMapp app, which flagged a rare genetic metabolic disease (glutaric acidemia type 1) in my 17 year old daughter. GenoMapp brought this serious health issue to our attention
Muy buena!
Muy importante conocer esta información
