CPC G16H 10/60 (2018.01) [G16B 20/00 (2019.02); G16B 20/20 (2019.02); G16B 45/00 (2019.02); G16B 50/00 (2019.02); G16B 50/30 (2019.02)] | 14 Claims |
1. A method comprising:
receiving data, the data identifying medical information;
determining, by a processor, an internal medical code associated with the medical information, the internal medical code being a non-genetic code, the internal medical code being machine readable and independent of genetic information;
determining, by a processor, genetic variants associated with the internal medical code, the determined genetic variant comprising a chromosome, the determined genetic variant being determined from a first database storing data identifying a plurality of genetic variants;
generating, by a processor, a graphical user interface, the graphical user interface displaying at least one of the determined genetic variants, the identity of a gene, and a location of the gene within the chromosome, the graphical user interface comprising a selectable link connecting the displayed genetic variant to further information associated with the displayed genetic variant;
presenting the genetic variants in a graphical format using a computing device; and
upon selecting the selectable link:
retrieving data over the Internet from a second database, the data related to the gene; and
modifying the graphical user interface to present the further information associated with the displayed genetic variant.
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