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AT HOME MEDICAL TESTS

You will find a multitude of in-home tests on this site. All shipped to you the next day confidentially with results in a couple of days. Save the embarrassment of going to a lab or doctor and order right here with complete privacy.

WE SPECIALIZE IN STD AND GENE MEDICAL TESTS.

SOME OF OUR TSTS INCLUDE:

HIV TEST, STD TESTS CHLAMYDIA TEST GONORRHEA TEST and UNIQUE GENE TESTS LIKE:

ALZHEIMERS TEST, THROMBOSIS TEST, NUTRITION TESTS, DIABATES TEST SKIN TESTCARDIOVASCULAR GENE TEST, and NARCOLEPSY TESTS

WHAT IS A AT HOME MEDICAL TEST?

An at-home medical test is a diagnostic or screening test that you can perform yourself at home, rather than visiting a doctor’s office or lab. These tests typically include a kit with instructions, sample collection materials (such as swabs, urine cups, or blood lancets), and sometimes a prepaid envelope to send the sample to a lab for analysis.

Types of At-Home Medical Tests:

HOW DOES A AT HOME MEDICAL TEST WORK?

At-home medical tests work by allowing you to collect a sample (such as saliva, urine, blood, or a swab) and either analyze it yourself using a test kit or send it to a lab for professional analysis. Here’s how they generally work:

  1. 1) Choose the Right Test

  • ->There are various at-home tests for different purposes, including pregnancy tests, COVID-19 tests, DNA tests, cholesterol tests, and more.
  • ->Some provide immediate results, while others require lab processing.
  1. 2)Sample Collection

  • The kit will include instructions on how to properly collect a sample. Common methods include:
    • ->Swabs: Used for COVID-19, flu, or strep throat tests.
    • ->Urine samples: Used for pregnancy, drug tests ,STD  or kidney function tests.
    • ->Blood samples: Often obtained via a finger prick for glucose, cholesterol, or food sensitivity tests and some STD tests
    • ->Saliva samples: Common for DNA and hormone tests.
  1. 3)Test Processing

  • ->Instant tests (Rapid Tests): Some tests, like pregnancy and COVID-19 antigen tests, provide results within minutes.
  • ->Lab-Processed Tests: Some tests require you to mail your sample to a certified lab for analysis. You typically receive results online or through an app within a few days.
  1. 4)Reviewing the Results

  • Test results may show:
    • ->Positive/Negative: Common in pregnancy and COVID-19 tests.
    • ->Levels or Ranges: Cholesterol, glucose, or hormone tests often give numerical results.
    • ->Genetic Information: DNA tests provide detailed ancestry or health risk data.
  1. 5)Follow-Up

  • ->If you receive a positive or concerning result, it’s usually recommended to follow up with a healthcare provider for confirmation and guidance.

How do I test myself with FASTDNATEST at-home STD tests?

Why should I take an STD test?

Many STDs are quite common but do not cause any symptoms, particularly in the early stages. However, despite being asymptomatic, infected individuals can still transmit the STD onto any sexual partners. In addition, if the STD is left untreated, serious health complications can occur. 

CDC recommendations for STD testing include:

What test types are used for STD tests?

When will my STD test results be ready?

The turnaround time for our tests depend on the type of test being performed. Please see the below list for the estimated testing times of our tests, calculated from the day after the laboratory receives your sample(s).

  • =>STD Health Tests: 1-3 business days

Please note that delays may occur during peak season. In addition, the #1 priority of the laboratory is the quality of the testing and the absolute accuracy of the results. The estimated turnaround times cannot be guaranteed if an exception is encountered, and the laboratory will not under any circumstances sacrifice the quality of the test in order to speed up the turnaround time. If additional testing is required, the test may take longer than the times indicated above.

What is the our HIV Test?

The At Home HIV Test Kit 4G is an advanced 4th generation test that brings you early detection with accurate and comprehensive results in the privacy of your own home. Simply collect your sample, mail it to the lab, and receive your results through a secure online portal in just a few days. It’s easy, fast and discreet.

What’s tested:

  • 1)HIV p24 antigen
  • 2)HIV I & II antibodies

Benefits of 4G HIV Tests

This 4th generation (4G) HIV test is a laboratory test that can detect HIV with more accuracy and at an earlier stage than 2nd generation rapid HIV tests. This test can be taken as soon as 1 month after a risk event. Early detection is important so you can get treatment and prevent transmitting HIV to others.

  • ->Greater accuracy
    More than 99.9% for positive detection
  • ->Earlier detection
    Detects infection up to 2 months sooner than a 2nd generation HIV test
  • ->Comprehensive results
    Detects the presence of HIV-1 & HIV-2 antibodies AND p24 antigen

Benefits of At-Home HIV Testing

  • ->Results in 1-2 business days* 
  • ->Convenient sample collection
    Collect your samples in the privacy of your own home. 
  • ->CAP Accredited, CLIA Certified
    Take comfort in knowing that your test will be conducted by our CAP-accredited, high complexity CLIA-certified laboratory.
  • ->Physician approved
    All tests are reviewed and approved by independent board-certified physicians 
  • ->Free physician consultation
    An independent physician network oversees the entire testing process. If you test positive for HIV, you will have the opportunity to discuss your test results directly with a board-certified physician at no extra cost. 
  • ->Online account
    Convenient online portal to securely check your test status and download your results.
  • ->100% confidentiality
    Your privacy is important to us. Our laboratory is HIPAA-compliant and we ensure that all personal information and data is secure. 

Who should get tested?

The CDC recommends everyone between the ages of 13 and 64 to get tested for HIV at least once.

HIV testing is also recommended if:

  • ->You are having sex with a new partner
  • ->You have been diagnosed with another sexually transmitted disease
  • ->You had a tattoo, piercing or acupuncture with unsterilized equipment
  • ->You are pregnant or considering becoming pregnant
  • ->You are in a high-risk group (injectable drug use, multiple sex partners, men who have sex with men)

WHAT IS OUR CHLAMYDIA GONORRHEA  AT HOME TEST?

This at-home chlamydia and gonorrhea test is an easy and convenient way to test for two of the most common sexually transmitted infections. With a simple urine sample, you can get the results you need in just 1 to 3 business days. Take charge of your sexual health and get tested for STDs today.

Measures:

  • =>Chlamydia
  • =>Gonorrhea

Collection Method: Urine

We offers STDs tests to screen for Chlamydia, Gonorrhea, Trichomoniasis, HIVHepatitis BHepatitis C, and Syphilis. These tests are available as individual tests and small combination tests, as well as the Complete STD Test, which covers all of the seven STDs screened by us.

Our at-home STD test kit is a convenient, discreet, and reliable way to check for three common sexually transmitted diseases.

Includes:

  • Chlamydia Test
  • Gonorrhea Test
  • Trichomoniasis Test

Collection Method: Urine

Convenient at-home STD test to check for four common sexually transmitted diseases (STDs).

Measures:

  • Chlamydia
  • Gonorrhea
  • Trichomoniasis
  • HIV (HIV-1/2 antibodies, p24 antigen)

Collection Method:
Fingerprick Blood, Urine

  1. Variants in two genes (CYP2R1 and GC) that influence vitamin D levels. Vitamin D is required for the normal mineralization of bone, and deficiency can increase the risk of osteoporosis. 
  2. WNT16 variant linked to bone formation
  3. COL1A1 variant linked to collagen production
  4. GDF5 variant linked to bone and cartilage development
  • PPARD - ability to burn fat for energy
  • VEGFA - ability to deliver oxygen to muscles
  • ACE - effect of blood pressure on endurance
  • ADRB2 - effect of adrenaline on endurance
  • PPARA - proportion of slow-twitch versus fast-twitch muscle fibers
  • ACTN3 - the "sprinter" gene
  • AGT - angiotensinogen and power ability
  • ACVR1B - the "muscle strength" gene
  • IL6 - the "muscle mass" gene
  • PPARGC1A - ability to increase aerobic capacity
  • PPARD - HDL-C "good cholesterol" response
  • MCT1 - using lactate for energy
  • BDNF - exercise motivation
  • CRP - heart rate recovery
  • COL1A1 - soft tissue injury risk
  • COL5A1 - risk for Achilles tendinopathy
  • COMT - pain tolerance

The DNA Skin Health Test is a very detailed genetic analysis of multiple different genes and variants that influence the health of your skin. Some variants influence the risk of different aspects of skin health (e.g. FLG variants affect the risk of eczema and dry skin), while others are more specific to one category. The skin health categories and analyzed genes are listed here. 

  • Collagen breakdown - MMP1, MMP3 
  • Glycation protection - GLO
  • Oxidative damage - GPX1, NQO1
  • Age spots - IRF4, MC1R, RALY
  • Eczema - FLG
  • Ichthyosis vulgaris (dry skin) - FLG
  • Psoriasis - HLA-C, IL23R, MTHFR, TNFAIP3, TNIP1, IL12B, IL13, LCE3D
  • Rosacea - HLA
  • Cellulite - ACE, HIF1A
  • Stretch marks - ELN
  • Varicose veins - MTHFR
  • Freckles - BNC2, ASIP, IRF4, MC1R, TYR
  • Tanning response - TYR, ASIP, IRF4, MC1R, SLC45A2

What is Hemochromatosis?

Hereditary Hemochromatosis is a genetic disorder that causes the body to absorb and store too much iron. The excess iron builds up in the body’s organs over time and eventually leads to organ damage. If hemochromatosis is not detected and treated early, it may eventually cause serious irreversible disorders such as arthritis, liver disease, heart disease and diabetes later in life.

Early detection can prevent future complications

Since hemochromatosis is treatable if detected early, screening for hemochromatosis can prevent potentially fatal complications from occurring. DNA testing for hemochromatosis is fast, simple and inexpensive.

The best time to get tested is before 30 years of age, so that the disease can be detected before organ damage occurs. When detected and treated early, there is a good chance of avoiding life-threatening complications of iron build up in the body later in life. If any family members test positive for hemochromatosis, other family members should also be tested.

Alzheimer’s disease is a progressive brain disorder characterized initially by memory loss and later by the loss of thinking, reasoning and behavioural abilities. There are both early-onset and late-onset forms of Alzheimer’s disease. The late-onset form occurs in 90% of Alzheimer’s disease cases and the first symptoms generally appear after 65 years of age.

The APOE gene is the biggest genetic risk factor linked to the late-onset form of Alzheimer’s disease. The late-onset Alzheimer’s disease APOE genetic test determines the APOE alleles that an individual has inherited. These alleles indicate whether an individual has an increased lifetime risk of developing late-onset Alzheimer’s disease. To follow are all of the possible allele results and their associated risk:

Neutral (homozygous e3 / e3) A neutral result means that the person carries two copies of the APOE e3 allele. This is the most common allele and is a neutral allele, meaning there is no increased or decreased risk of Alzheimer’s with the presence of this allele. There is a 100% chance that this person will pass the neutral APOE e3 allele to the next generation and there is no chance that this person will pass the high risk e4 allele to the next generation.

Reduced Risk (homozygous e2 / e2) A reduced risk (homozygous) result means that the person has inherited two copies of the APOE e2 allele and may have a slightly reduced risk of Alzheimer’s. There is a 100% chance that this person will pass the reduced risk APOE e2 allele to the next generation and there is no chance that this person will pass the high-risk e4 allele to the next generation.

Reduced Risk (heterozygous e2 e3) A reduced risk (heterozygous) result means that the person has inherited one copy of the APOE e2 allele and one copy of the neutral APOE e3 allele. This person may have a slightly reduced risk of Alzheimer’s. There is a 50% chance that they will pass the reduced risk APOE e2 allele to the next generation and a 50% chance that they will pass the neutral APOE e3 allele to the next generation. There is no chance that this person will pass the high-risk e4 allele to the next generation.

Increased Risk (heterozygous e2 e4 or e3 e4) An increased risk (heterozygous) result means that the person has inherited one copy of the APOE e4 allele and one copy of either the APOE e2 or APOE e3 allele. This person has a 3-fold increased risk of developing Alzheimer’s. This person has a 50% chance of passing the defective gene (APOE e4 allele) to the next generation. If two heterozygous affected individuals have children, there is a 25% chance that their children will be normal, a 50% chance that their children will also be heterozygous affected, and a 25% chance that their children will inherit two defective genes and be at an even higher risk of developing Alzheimer’s. Increased Risk (homozygous e4 e4) An increased risk (homozygous) result means that the person has inherited two copies of the APOE e4 allele, one from each parent. This person has 10 – 15 times the normal risk of developing Alzheimer’s. There is a 100% chance that an affected individual with a homozygous genotype will pass the APOE e4 allele to the next generation.

 

What genetic variant do we check for narcolepsy?

Multiple genetic variants have been identified that are associated with cardiovascular disease. Genetrace offers a comprehensive DNA Cardiovascular Health Test that analyzes variants in 27 genes (listed below), which each affect different aspects of cardiovascular health.

Triglycerides – main form of fat (or lipid) found in the body:

HDL cholesterol – considered “good” cholesterol):

  • CETP
  • LCAT
  • LPL
  • ANGPTL4
  • GALNT2
  • LIPG
  • MMAB
  • HNF4A

Other aspects of cardiovascular health, including lipoprotein(a) levels, lipid metabolism, cell proliferation, and processing of unsaturated fats, are affected by variants in the following genes/regions:

  • LPA
  • APOA5/A4/C3/A1
  • LIPC
  • FADS1
  • 9p21
  • GCKR

 

What genes are tested in our DNA Nutrition Test?

  • Vitamin A – BCO1
  • Vitamin B6 – NBPF3
  • Folate (Vitamin B9) – MTHFD1 and MTHFR
  • Vitamin B12 – FUT2 
  • Vitamin C – SLC23A1
  • Vitamin D – CYP2R1 and GC
  • Vitamin E – APOA5
  • Iron – TF and TMPRSS6
  • Omega-3 – NOS3

What genetic variants are tested in our  DNA Thrombotic Risk Test?

 

Genetic changes in three genes are analyzed in the thrombotic risk test. Each change contributes to an increased risk of thrombosis. 

  • F5 – the Factor V Leiden mutation (1691G>A)
  • F2 – the prothrombin mutation (20210G>A)
  • MTHFR – two mutations (677C>T and 1298A>C)

How do your genes influence your likelihood of losing weight?

Genetic variation plays a big role in every individual’s body weight and ability to lose weight. This variation can affect everything from how much you snack, to exercise motivation and metabolic circadian rhythm. The DNA Weight Loss Test identifies variants in the following genes.

  • Snacking – MC4R
  • Food disinhibition – NMB
  • Hunger – FTO
  • Satiety – SH2B1
  • Exercise motivation – BDNF
  • BMI and physical exercise – FTO
  • Fat breakdown in response to exercise – ADRB2
  • Sensitivity to saturated fats – APOA2
  • Fatty acid uptake – FABP2
  • Starch digestion – AMY1
  • Adiponectin levels – ADIPOQ
  • Metabolic circadian rhythm – CLOCK

What is included in our DNA Type 2 Diabetes Gene Test?

Type 2 diabetes is becoming a highly prevalent disease worldwide. By 2030, an estimated 1 in 10 people will be diagnosed with type 2 diabetes. Obesity, inactivity, age, family history, ethnicity, as well as genetics, can increase the risk of type 2 diabetes. 

The aspects of health related to type 2 diabetes risk and the associated genes are listed here:

  • Hunger and Satiety – FTO
  • Sugar Intake – GLUT2
  • Fatty Acid Uptake – FABP2
  • Fatty Acid Processing – FADS1
  • Antioxidants – SOD2
  • Glucose Release – G6PC2 
  • Glucokinase Enzyme – GCKR
  • Proinsulin Conversion – MADD
  • Insulin Secretion – TCF7L2, HNF4A
  • Insulin Sensitivity – ACC2, IRS1
  • Glucose-Stimulated Insulin Release – ADCY5
  • Beta Cell Development – PROX1, GLIS3
  • Beta Cell Function – GCK
  • Adiponectin Levels – ADIPOQ
  • Hormone Levels – SHBG
  • Zinc Transport – SLC30A8
  • Circadian Rhythms – CRY2, MTNR1B
  • Hypoxia – HIF1A

Please note that this test does not diagnose type 2 diabetes. Type 2 diabetes is a complex disease fuelled by a combination of factors. Genetic variants identified in the test are only part of the risk factors that can influence your likelihood of developing type 2 diabetes. It is possible to inherit genetic variants with contradicting effects, but it is the combined effect of these variants, along with diet and lifestyle factors that will influence your overall risk of type 2 diabetes. 

 

What genes are tested in the DNA Skin Health Test?

The DNA Skin Health Test is a very detailed genetic analysis of multiple different genes and variants that influence the health of your skin. Some variants influence the risk of different aspects of skin health (e.g. FLG variants affect the risk of eczema and dry skin), while others are more specific to one category. The skin health categories and analyzed genes are listed here. 

  • Collagen breakdown – MMP1, MMP3 
  • Glycation protection – GLO
  • Oxidative damage – GPX1, NQO1
  • Age spots – IRF4, MC1R, RALY
  • Eczema – FLG
  • Ichthyosis vulgaris (dry skin) – FLG
  • Psoriasis – HLA-C, IL23R, MTHFR, TNFAIP3, TNIP1, IL12B, IL13, LCE3D
  • Rosacea – HLA
  • Cellulite – ACE, HIF1A
  • Stretch marks – ELN
  • Varicose veins – MTHFR
  • Freckles – BNC2, ASIP, IRF4, MC1R, TYR
  • Tanning response – TYR, ASIP, IRF4, MC1R, SLC45A2