In the Epi23 report, the origins of the person are enlightened using an algorithm. At the same time, the genome of the person is compared with the data obtained from Neanderthal specimens and the similarity rate is calculated. The predispositions of the person are found through lists created by experts. Findings are detected and reported using disease-specific panels (autoimmune, cardiology, epilepsy, food allergy). Changes in genes reported by ACMG incidental findings are detected and reported. In addition, the heterozygous and homozygous findings of the individual are presented along with the diseases specified by ClinVar. In order to find a reaction to any drug, the genome of the person is analyzed and the findings are reported.