CircaGene Services and Report

Reading your

  • Reading ALL chromosomes
    (with option of CLINICAL-GRADE Service)
  • or only genes
    (Partial information but Cost-effective)

Applying our
Genetic Sonar

  • With EACH Whole Sequencing, CircaGene provides a First-pass analysis on all DNA Data to establish a first Ranking of main Predispositions.

Deep Analysis of
Your risks

  • DEEP ANALYSIS per Risk
  • APPLICATION of EXPERT Disease-Specific Analysis


  • A Marketplace provides Users all tools to mitigate their individual Health Risks

CircaGene DEFINITIVE solution for Genetic Data Analysis

Two methods, whole exome sequencing and whole genome sequencing, are increasingly used in healthcare and research to identify genetic variations. Continued study of exome and genome sequences can help determine whether new genetic variations are associated with health conditions, which will aid disease diagnosis in the future. More detailed information about WES and WGS sequencing :

The resources on this site should not be used as a substitute for professional medical care or advice. Users with questions about a personal health condition should consult with a qualified healthcare professional.

What Information CircaGene Gives you ?

Analysis of YOUR risks

Included risks searched for :

ARSACS genetic disorder
Agenesis of the Corpus Callosum with Peripheral Neuropathy
Age-Related Macular Degeneration
Alpha-1 Antitrypsin Deficiency
Autosomal Recessive Polycystic Kidney Disease
Beta Thalassemia and Related Hemoglobinopathies
Bloom Syndrome
BRCA1/BRCA2 (Selected Variants)
Canavan Disease
Celiac Disease
Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)
Cystic Fibrosis
D-Bifunctional Protein Deficiency
Dihydrolipoamide Dehydrogenase Deficiency
Familial Dysautonomia
Familial Hypercholesterolemia
Familial Hyperinsulinism (ABCC8-Related)
Familial Mediterranean Fever
Fanconi Anemia Group C
G6PD Deficiency
Gaucher Disease Type 1
Glycogen Storage Disease Type Ia
Glycogen Storage Disease Type Ib
GRACILE Syndrome
Hereditary Amyloidosis (TTR-Related)
Hereditary Fructose Intolerance
Hereditary Hemochromatosis (HFE-Related)
Hereditary Thrombophilia
Herlitz Junctional Epidermolysis Bullosa (LAMB3-Related)
Late-Onset Alzheimer's Disease
Leigh Syndrome, French Canadian Type
Limb-Girdle Muscular Dystrophy Type 2D
Limb-Girdle Muscular Dystrophy Type 2E
Limb-Girdle Muscular Dystrophy Type 2I
Maple Syrup Urine Disease Type 1B
MCAD Deficiency
Mucolipidosis Type IV
MUTYH-Associated Polyposis
Neuronal Ceroid Lipofuscinosis (CLN5-Related)
Neuronal Ceroid Lipofuscinosis (PPT1-Related)
Niemann-Pick Disease Type A
Nijmegen Breakage Syndrome
Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)
Parkinson's Disease
Pendred Syndrome and DFNB4 Hearing Loss (SLC26A4-Related)
Phenylketonuria and Related Disorders
Primary Hyperoxaluria Type 2
Rhizomelic Chondrodysplasia Punctata Type 1
Salla Disease
Sickle Cell Anemia
Sjogren-Larsson Syndrome
Tay-Sachs Disease
Type 2 Diabetes
Tyrosinemia Type I
Usher Syndrome Type 1F
Usher Syndrome Type 3A
Zellweger Syndrome Spectrum (PEX1-Related)

Your Health is our priority