DNA Health Test

This 24Genetics Health Report could make a real difference in your wellbeing.

 

Our genetic information is key to making some of the most important decisions in our lives. Some diseases we can prevent if we act in time, and our DNA can help us to identify them. Prevention and early diagnosis can multiply success ratios by 5 to 10 times. Your genomics will tell you where you should focus. By analyzing your genetic map, we obtain essential information so that you can make the best decisions regarding your health and wellbeing.

DNA Health Test 

Reports available in English, German, French, Italian, and Spanish 

There is a lot of useful information in this Genetic Test, giving you the opportunity to prevent the transmission of several monogenic diseases to your future children. Some of these diseases may be present in your genes and, even if you do not suffer them, they may develop in your children or grandchildren. With the genetic map, we can identify some of them so that we can prevent them, or you can enjoy the peace of mind of knowing that you do not carry those genes. Your genetic map will also help your doctor to prescribe the most suitable drugs, because you will know which ones are best for you, based on your genetic predisposition.

This 24Genetics Panel is one of the most advanced tests on the market. It employs the latest Illumina technology and can give us a considerable amount of information, with a high degree of reliability.

This gene panel is, without a doubt, the best value for your money. We analyze 700,000 genetic markers covering the scientific community’s most important findings. Furthermore, we also examine many genetic markers that are now the subject of research, and that will be endorsed by scientific evidence in the coming months or years. Thus, you can sequence your genes today, and the data extracted will be valid and valuable not just today, but tomorrow too.

At a much lower price than that for complete genome sequencing, this genetic test offers the analysis of genetic markers for more than 200 diseases, genetic predisposition to dozens of medicines, and a wealth of information pertinent to your health care.

Most of the Gene Panels that one can find on the market rely on 2,500 to 5,000 genetic markers, while our new 24Genetics Panel analyses 700,000.

At this point in time, we have not found any more complete genetic test at this price. Buy now:

DNA Health Test

The 24Genetics DNA Health Test report includes the following sections:

We analyze your genetic predisposition to more than 200 diseases, grouped into these types:

(click here to see the list of diseases)

Genetic Health Risks: Gwas

In this part, we apply GWAS publications about Polygenic Diseases. This kind of studies compares the DNA markers of people with a disease or trait, to people without it. These studies can be beneficial for prevention and early diagnosis. It is not a diagnostic tool, but it helps one to see where he needs to be more careful, indicating his predisposition compared to the rest of the population. 

Click here to watch this interesting Illumina Video about this kind of predispositions

Genetic Health Risk: mutations

In this section, we analyse the mutations of the most important genes from the oncological point of view. We look for mutations suspected of being pathogenic, specifically those reported as pathogenic in the ClinVar database.

Carrier Status

Hereditary diseases are likely to be passed on to your offspring. In most cases, we can be carriers, and never suffer the disease, but there is a risk that our progeny will suffer them if certain conditions exist. These are mostly monogenic diseases. In this group, we are looking for pathogenic mutations, or likely pathogenic mutations, in the genes involved in these diseases. We look for the mutations that are reported in some of the most important genetic databases worldwide, primarily the OMIM and ClinVar. In the event that you have this kind of mutation or inheritable diseases in your family, taking this kind of genetic test is very important. With the DNA data, a geneticist can give you guidelines on how to act. 

Biomarkers, biometrics, and traits

In this section we use, again, the GWAS statistical analysis to calculate your genetic predisposition to present abnormal levels of certain metabolic parameters. We will tell you what your genes indicate that you have to be careful with. There are mutations that predispose one to have abnormal cholesterol or triglyceride levels, or other important parameters so that you can monitor them more closely. You can also view your predisposition to the effects of alcohol, caffeine and more

Pharmacogenetics

We will analyze the mutations that predispose you to have certain medications work well or not in your body. This will help your doctors to choose the right medicines for you. Your pharmacological analysis will be your first step into personalized medicine. 

The Mayo Clinic and Pharmacogenomics: Click here to see the video


The genetic information provided by 24genetics is valid only for research, information and educational uses. In no case, the test information is valid for clinical use. At 24Genetics we advise all our customers to schedule a Genetic Advice Consultation to gain a proper understanding of the DNA Reports and get the most out of them.

 health dna report

Download our DNA Health Report Sample 

Reports available in English, German, French, Italian and Spanish 

EN ancestry free

 

Questions and answers 

 

This 24Genetics Health Report could make a real difference in your wellbeing.

 

Our genetic information is key to making some of the most important decisions in our lives. Some diseases we can prevent if we act in time, and our DNA can help us to identify them. Prevention and early diagnosis can multiply success ratios by 5 to 10 times. Your genomics will tell you where you should focus. By analyzing your genetic map, we obtain essential information so that you can make the best decisions regarding your health and wellbeing.

DNA Health Test 

Reports available in English, German, French, Italian, and Spanish 

There is a lot of useful information in this Genetic Test, giving you the opportunity to prevent the transmission of several monogenic diseases to your future children. Some of these diseases may be present in your genes and, even if you do not suffer them, they may develop in your children or grandchildren. With the genetic map, we can identify some of them so that we can prevent them, or you can enjoy the peace of mind of knowing that you do not carry those genes. Your genetic map will also help your doctor to prescribe the most suitable drugs, because you will know which ones are best for you, based on your genetic predisposition.

This 24Genetics Panel is one of the most advanced tests on the market. It employs the latest Illumina technology and can give us a considerable amount of information, with a high degree of reliability.

This gene panel is, without a doubt, the best value for your money. We analyze 700,000 genetic markers covering the scientific community’s most important findings. Furthermore, we also examine many genetic markers that are now the subject of research, and that will be endorsed by scientific evidence in the coming months or years. Thus, you can sequence your genes today, and the data extracted will be valid and valuable not just today, but tomorrow too.

At a much lower price than that for complete genome sequencing, this genetic test offers the analysis of genetic markers for more than 200 diseases, genetic predisposition to dozens of medicines, and a wealth of information pertinent to your health care.

Most of the Gene Panels that one can find on the market rely on 2,500 to 5,000 genetic markers, while our new 24Genetics Panel analyses 700,000.

At this point in time, we have not found any more complete genetic test at this price. Buy now:

DNA Health Test

The 24Genetics DNA Health Test report includes the following sections:

We analyze your genetic predisposition to more than 200 diseases, grouped into these types:

(click here to see the list of diseases)

Genetic Health Risks: Gwas

In this part, we apply GWAS publications about Polygenic Diseases. This kind of studies compares the DNA markers of people with a disease or trait, to people without it. These studies can be beneficial for prevention and early diagnosis. It is not a diagnostic tool, but it helps one to see where he needs to be more careful, indicating his predisposition compared to the rest of the population. 

Click here to watch this interesting Illumina Video about this kind of predispositions

Genetic Health Risk: mutations

In this section, we analyse the mutations of the most important genes from the oncological point of view. We look for mutations suspected of being pathogenic, specifically those reported as pathogenic in the ClinVar database.

Carrier Status

Hereditary diseases are likely to be passed on to your offspring. In most cases, we can be carriers, and never suffer the disease, but there is a risk that our progeny will suffer them if certain conditions exist. These are mostly monogenic diseases. In this group, we are looking for pathogenic mutations, or likely pathogenic mutations, in the genes involved in these diseases. We look for the mutations that are reported in some of the most important genetic databases worldwide, primarily the OMIM and ClinVar. In the event that you have this kind of mutation or inheritable diseases in your family, taking this kind of genetic test is very important. With the DNA data, a geneticist can give you guidelines on how to act. 

Biomarkers, biometrics, and traits

In this section we use, again, the GWAS statistical analysis to calculate your genetic predisposition to present abnormal levels of certain metabolic parameters. We will tell you what your genes indicate that you have to be careful with. There are mutations that predispose one to have abnormal cholesterol or triglyceride levels, or other important parameters so that you can monitor them more closely. You can also view your predisposition to the effects of alcohol, caffeine and more

Pharmacogenetics

We will analyze the mutations that predispose you to have certain medications work well or not in your body. This will help your doctors to choose the right medicines for you. Your pharmacological analysis will be your first step into personalized medicine. 

The Mayo Clinic and Pharmacogenomics: Click here to see the video


The genetic information provided by 24genetics is valid only for research, information and educational uses. In no case, the test information is valid for clinical use. At 24Genetics we advise all our customers to schedule a Genetic Advice Consultation to gain a proper understanding of the DNA Reports and get the most out of them.

 health dna report

Download our DNA Health Report Sample 

Reports available in English, German, French, Italian and Spanish 

EN ancestry free

 

Questions and answers 

 

IS THIS TEST AVAILABLE IN MY COUNTRY?

We send our DNA kits to any country in the world. You can choose free regular shipping by post, or Express Shipping (round trip). We have many warehouses worldwide, so we will ship from the closest point possible. Europe and USA feature free Express Shipping. Some Packs offer free Express Shipping worldwide

HOW CAN I TAKE THIS TEST?

is really simple. We will home deliver a DNA KIT to you. You will receive a small cotton swab that you simply rub inside your mouth. Watch this video before using the kit: Click here to see the video. After following a few simple instructions, send us the swab back. At a specialized laboratory, we extract the DNA from the sample that you have sent us, and we carry out a process in which we can read what is written in some 700,000 markers of your DNA. After a complex computer analysis, our algorithms apply the latest genetic studies to generate the report that we place in your hands.

SHOULD I MAKE DRASTIC CHANGES TO MY HEALTH TREATMENTS ON MY OWN BECAUSE OF THIS TEST RESULTS?

No. Any changes you plan to make regarding your health should be analyzed by an expert geneticist and specialized doctors. Any questions you have about any genetic test should be posed to healthcare personnel expert in Genetic Diagnosis.

DOES IT ALL DEPEND ON MY GENES?

No. Your body responds to a whole range of conditions. Our genes are certainly an important parameter, but the lifestyle, exercise, diet, and many other circumstances influence our bodies. Knowing yourself well certainly helps to treat your body in the most appropriate way. And this is what you can get from genetics: more knowledge.

ARE ALL THE TESTS OF THE SAME QUALITY?

No. Our genetic test is, possibly, the most complete on the market. There are some simple genetic tests that can only give you a small amount of information. Our genetic test is based on latest-generation genetic sequencing, allowing us to analyze about 700,000 genetic markers.

WHAT IS THIS TEST BASED ON?

This test is based on different genetic studies that are internationally recognized and accepted by the scientific community. There are certain scientific organizations and databases where studies are published when there exists a certain level of consensus. Our genetic tests are carried out by applying these studies to our customers’ genetic information. Below you can see some of these studies used in this genetic test.

 

 

DNA Health Test

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EN ancestry free

 

 

These are some of the Diseases you will find in our report:

 

Alopecia areata GLYCOGEN STORAGE DISEASE Ia; GSD1A
Intracranial aneurysm GLYCOGEN STORAGE DISEASE II; GSD2
Rheumatoid arthritis HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2; FHL2
Chronic bronchitis and chronic obstructive pulmonary disease HERMANSKY-PUDLAK SYNDROME 3; HPS3
Breast cancer GWAS HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME
Breast Cancer: pathogenic SNP carrier ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED
Ovarian cancer in BRCA1 mutation carriers JERVELL AND LANGE-NIELSEN SYNDROME 1; JLNS1
Prostate cancer JOUBERT SYNDROME 14; JBTS14
Prostate cancer aggressiveness JOUBERT SYNDROME 16; JBTS16
Prostate cancer (early onset) JOUBERT SYNDROME 3; JBTS3
Bladder cancer JOUBERT SYNDROME 5; JBTS5
Upper aerodigestive tract cancers JOUBERT SYNDROME 7; JBTS7
Basal cell carcinoma JOUBERT SYNDROME 8; JBTS8
Motion sickness JOUBERT SYNDROME 9; JBTS9
Primary biliary cirrhosis KABUKI SYNDROME 1; KABUK1
Age-related macular degeneration LEIGH SYNDROME; LS
Conduct disorder LEOPARD SYNDROME 1; LPRD1
Type 1 diabetes LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM
Type 1 diabetes nephropathy LISSENCEPHALY 1; LIS1
Type 2 diabetes LOEYS-DIETZ SYNDROME 2; LDS2
Endometriosis LONG QT SYNDROME 1; LQT1
Celiac disease LYNCH SYNDROME I
Alzheimer's disease (late onset) MAPLE SYRUP URINE DISEASE; MSUD
Coronary heart disease MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 2; MODY2
Parkinson's disease MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3; MODY3
Multiple sclerosis MECKEL SYNDROME, TYPE 3; MKS3
Systemic sclerosis MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH
Schizophrenia METACHROMATIC LEUKODYSTROPHY; MLD
Glioma METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE
Hypothyroidism METHYLMALONIC ACIDURIA, cblA TYPE
Myocardial infarction (early onset) METHYLMALONIC ACIDURIA, cblB TYPE
Chronic lymphocytic leukemia MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1; MC3DN1
Hodgkin's lymphoma MUCOPOLYSACCHARIDOSIS TYPE VI; MPS6
Diffuse large B cell lymphoma MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7
Follicular lymphoma MUCOPOLYSACCHARIDOSIS, TYPE IIIA; MPS3A
Myasthenia gravis MUCOPOLYSACCHARIDOSIS, TYPE IIIB; MPS3B
Multiple myeloma MUCOPOLYSACCHARIDOSIS, TYPE IVA; MPS4A
Neuroblastoma MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1
Osteosarcoma MYOPATHY, MYOFIBRILLAR, 1; MFM1
Psoriasis MYOPATHY, CENTRONUCLEAR, 1; CNM1
Allergic sensitization MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX
Testicular germ cell tumor NEMALINE MYOPATHY 2; NEM2
Wilms tumor CYSTINOSIS, NEPHROPATHIC; CTNS
Vitiligo NIEMANN-PICK DISEASE, TYPE C1; NPC1
17-BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY NIEMANN-PICK DISEASE, TYPE A
3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D NIEMANN-PICK DISEASE, TYPE B
AARSKOG-SCOTT SYNDROME; AAS NOONAN SYNDROME 1; NS1
ACHROMATOPSIA 2; ACHM2 NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA; NSLL
LEUKEMIA, ACUTE MYELOID; AML NOONAN SYNDROME 4; NS4
ADRENOLEUKODYSTROPHY; ALD Obesity due to melanocortin 4 receptor deficiency
HYPOPHOSPHATASIA, ADULT ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B
ALLAN-HERNDON-DUDLEY SYNDROME; AHDS OSTEOGENESIS IMPERFECTA, TYPE III; OI3
ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD DIABETES MELLITUS, PERMANENT NEONATAL; PNDM
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED PITT-HOPKINS SYNDROME; PTHS
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY POLYMICROGYRIA, BILATERAL FRONTOPARIETAL; BFPP
ANGELMAN SYNDROME; AS MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE; MCPH5
ANTITHROMBIN III DEFICIENCY; AT3D RETINITIS PIGMENTOSA; RP
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10 RUBINSTEIN-TAYBI SYNDROME 1; RSTS1
AURICULOCONDYLAR SYNDROME 1; ARCND1 SOTOS SYNDROME 1; SOTOS1
HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT; ADHR SUPRAVALVULAR AORTIC STENOSIS; SVAS
BARDET-BIEDL SYNDROME 1; BBS1 TAY-SACHS DISEASE; TSD
MUSCULAR DYSTROPHY, BECKER TYPE; BMD TUBEROUS SCLEROSIS 1; TSC1
BETA-THALASSEMIA TUBEROUS SCLEROSIS 2; TSC2
BLOOM SYNDROME; BLM ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A
BRUGADA SYNDROME 1; BRGDA1 TYROSINEMIA, TYPE I; TYRSN1
CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1 USHER SYNDROME, TYPE I; USH1
CARDIOMYOPATHY, DILATED, 1S; CMD1S USHER SYNDROME, TYPE ID; USH1D
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1 USHER SYNDROME, TYPE IF; USH1F
CEROID LIPOFUSCINOSIS, NEURONAL, 1; CLN1 USHER SYNDROME, TYPE IIA; USH2A
CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7 USHER SYNDROME, TYPE IIC; USH2C
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C USHER SYNDROME, TYPE IID; USH2D
CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE; CDPX1 USHER SYNDROME, TYPE IIIA; USH3A
GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF; ACADVLD
ADRENAL HYPOPLASIA, CONGENITAL; AHC VON HIPPEL-LINDAU SYNDROME; VHL
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C WEAVER SYNDROME; WVS
CORNELIA DE LANGE SYNDROME 1; CDLS1 Wilson Disease
COSTELLO SYNDROME; CSTLO AGAMMAGLOBULINEMIA, X-LINKED; XLA
CYSTIC FIBROSIS; CF  
DANON DISEASE  
DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1A  
DEAFNESS, AUTOSOMAL RECESSIVE 31; DFNB31  
DEAFNESS, AUTOSOMAL RECESSIVE 7; DFNB7  
DEAFNESS, AUTOSOMAL RECESSIVE 9; DFNB9  
MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA  
CARDIOMYOPATHY, DILATED, 1A; CMD1A  
DUBIN-JOHNSON SYNDROME; DJS  
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2
MYOCLONIC EPILEPSY OF LAFORA  
ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2  
FABRY DISEASE  
FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1  
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2
FAMILIAL MEDITERRANEAN FEVER; FMF  
THYROID CARCINOMA, FAMILIAL MEDULLARY; MTC
FANCONI ANEMIA, COMPLEMENTATION GROUP O; FANCO
NEPHROTIC SYNDROME, TYPE 1; NPHS1  
GAUCHER DISEASE, TYPE I  
GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1  
GLUTARIC ACIDEMIA I; GA1  
MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY; MADD

 

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