$250
Want to know if you have the genes associated with celiac disease? Most individuals with celiac disease have at least one genetic risk variant. In fact, a negative result means there is less than a 0.04% chance you will develop celiac disease in your lifetime. Discover your risk through our DNA test.
Celiac disease is an autoimmune disorder triggered by gluten, a protein present in wheat, barley, rye, and other grains. Many processed foods also contain gluten.
If someone with celiac disease eats gluten, their immune system responds by damaging the lining of their intestines. This damage prevents proper nutrient absorption, which can lead to malnutrition and other health complications.
Celiac disease is significantly associated with particular variants of two critical genes in the human immune system: HLA-DQA1 and HLA-DQB1.
This test identifies three high-risk variants of these genes:
Inheriting one or more of these variants increases your risk of developing celiac disease. However, having the variants does not guarantee you will get the disease.
While many individuals with these variants may develop celiac disease, not everyone will. Conversely, without these variants, the probability of getting celiac disease drops to less than 0.04%.
The test requires only a simple DNA sample from a mouth swab. No dietary changes are needed as it screens your inherent genetic makeup, not consumption of gluten. Results can help guide further discussion with your doctor about celiac disease screening options.
The symptoms of celiac disease differ among people. Whether the symptoms are mild or severe, the common factor is damage to the intestinal lining.
Common symptoms include:
Weight loss may happen because the body can’t absorb nutrients, or some people may gain weight from eating more to make up for this. Continued exposure to gluten can damage the intestines and also lead to other food sensitivities, such as lactose intolerance.
If the disease is not diagnosed and treated, more severe health issues can occur. These can include:
Other symptoms may include nosebleeds, hair loss, seizures, mouth ulcers, dental issues, irregular menstrual cycles, and tingling in the legs or feet. Osteoporosis is often seen in celiac patients due to poor absorption of calcium. The disease can also cause infertility, miscarriages, or birth defects because of poor folic acid absorption.
Celiac disease risk is influenced by the HLA genes found on chromosome 6. Each individual inherits two copies of these genes—one from each parent.
Most individuals with celiac disease have at least one genetic risk allele within their HLA genes. This DNA test identifies variations in three celiac disease (CD)-associated alleles present in the HLA-DQA1 and HLA-DQB1 genes: HLA-DQA105, HLA-DQB102, and HLA-DQB1*0302.
These specific alleles can combine to produce protein complexes known as DQ2 and DQ8. Their presence or absence provides insight into an individual’s risk of gluten sensitivity and CD. If none of these CD-associated alleles are found, the CD risk is notably low.
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From paternity tests to grandparent tests, we offer a wide range of DNA tests to fit your needs.
COLLECT SAMPLE
Easily swab the participants with our painless mouth swabs, then send the samples to our laboratory for analysis.
RECEIVE RESULTS
Access your confidential results online within 7-14 business days. Our team of experts is available for any questions.