Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Cost Of Celiac Genetic Test?


hazelnutty42

Recommended Posts

hazelnutty42 Rookie

If you've looked into this test, did your insurance cover it? If not, what was the cost out of pocket? Just curious. If my biopsy confirms Celiac I want both of my kids to have the genetic test. Thanks!


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



kareng Grand Master

I forget what it cost. You can call Quest Diagnostics and they will tell you. My doctor ordered it and insurance paid without a peep.

Edit- looked back at my old posts - it was about $260 from Quest about a year ago

StephanieL Enthusiast

If you have it, the kids chance of having the gene is fairly high so I'm not sure I would spend the money on doing it if your insurance doesn't cover it.  We were told not to bother with the younger sibs because of the same reason.  It isn't diagnostic so it won't really help for anything other than curiosity.

SMRI Collaborator

The gene testing really won't tell you much but you should have the kids testes for the IgA, IgG tests.  It's likely they will have one or more gene but that doesn't mean they are Celiac.  If you are going to spend the money, spend it on the other testing first.  

kareng Grand Master

I just did my test for fun. I wanted to know how many genes I had so I could kind of, un scientifically, see what my boys chances are. I was happily surprised that my insurance paid for it. I did not have my boys tested because I didn't want that in their medical records as it could limit their career choices and perhaps be a " pre-existing" condition some day.

Noobette Apprentice

23andme testing is $99. It takes a lot of figuring out, but I was able to determine that I carry both HLA-Dq2.5 and HLA-Dq8.

kareng Grand Master

I would be careful with the 23 and me testing. They have had some legal issues.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



ezgoindude Explorer

I live in Arizona, I was at the time I was still a dependent under united health care with my parents.  The HLA genetic marker test was through Labcorp,  I only paid $28.73 with my parents insurance,  the original bill showed $750.00.

hazelnutty42 Rookie

Thanks everyone. I was thinking the genetic test because I know my kids don't currently have celiac. They are 7 and 9. So a TTG IgA would be useless right? I don't need to confirm a diagnosis, but was under the impression the gene would let us know that we have it coming up. 

kareng Grand Master

The gene just means you can get it. But, about 30% of people have a Celiac gene.... And they think about 1% have celiac. So, all it would do is rule it out.

Open Original Shared Link

"Genetics don’t diagnose celiac disease. They do, however, clarify whether an individual is “at-risk” for it. If this is the case, you should closely monitor your symptoms and submit to blood tests every 2-3 years or immediately upon the sight of symptoms. ..."

StephanieL Enthusiast

Any first degree relatives should be tested every 3 years OR if they have symptoms.  Theres no way to know for sure they don't currently have it unless they are tested.

BlessedMommy Rising Star

Yes, they need to be tested. Celiac can be asymptomatic, so there's no way to be sure that they don't currently have it, without testing them.

GottaSki Mentor

My celiac doc tested me when initial celiac panels for my then 13 and 15 year olds came up neg with numberous symptoms. I'm double plus one. Couple years later the older one had genetic test when he was unsure of status....he too is double plus one...which means my non celiac husband carries at least one pesky DQ2....possibly a DQ8.

Sorry..original poster asked cost. When doctor ordered it is covered. Our coverage changed a bit .. So we did pay copayment with my son's test.

GottaSki Mentor

Thanks everyone. I was thinking the genetic test because I know my kids don't currently have celiac. They are 7 and 9. So a TTG IgA would be useless right? I don't need to confirm a diagnosis, but was under the impression the gene would let us know that we have it coming up.

They should have a complete celiac antibody panel every three years. Symptoms are numerous and at times vague. First degree relatives should always be tested every three years..more often if symptoms present.

frieze Community Regular

mostly because they (23 and me) were cutting into others revenue stream.....

SMRI Collaborator

Thanks everyone. I was thinking the genetic test because I know my kids don't currently have celiac. They are 7 and 9. So a TTG IgA would be useless right? I don't need to confirm a diagnosis, but was under the impression the gene would let us know that we have it coming up. 

 

How do you know they do not have Celiac?  They could just not be symptomatic yet.  My nice was tested as an add on to other testing and her TGG Iga was 130 with no symptoms at all.  She was also biopsy positive.  The gene testing is pretty much useless without the TTG IgA, IgG testing and perhaps biopsies.  I would get both kids tested for the TGG tests and then go from there.

hazelnutty42 Rookie

Thanks! This is helpful. I'll wait for my biopsy results and def have them tested based on that. This forum is very helpful. Thank you! 

RMJ Mentor

The idea of doing genetic testing of relatives is to rule out Celiac. If ruled out, that's it, no more testing. If it is not ruled out, antibody testing every few years.

StephanieL Enthusiast

The idea of doing genetic testing of relatives is to rule out Celiac. If ruled out, that's it, not more testing. If it is not ruled out, antibody testing every few years.

Drawing the genetics WITH the panel would be one thing but to do just the genetics means if it's + it'll still require another draw. Also many insurance companies won't do the genetics without the panel first.  Lastly, if a parent has Celiac, the chances of a kid having the gene is pretty high which doesn't tell ya much but that there is a predisposition.

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to Jmartes71's topic in Related Issues & Disorders
      21

      My only proof

    2. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      21

      My only proof

    3. - knitty kitty replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      44

      Supplements for those Diagnosed with Celiac Disease

    4. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      21

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,545
    • Most Online (within 30 mins)
      7,748

    PatientOne
    Newest Member
    PatientOne
    Joined

  • Celiac.com Sponsor (A20):



  • Celiac.com Sponsor (A22):




  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
    • knitty kitty
      @Scatterbrain, Thiamine Vitamin B1 and amino acid Taurine work together.  Our bodies can make Taurine from meats consumed.  Our bodies cannot make Thiamine and must consume thiamine from food.  Meat is the best source of B vitamins like Thiamine.   Vegetarians may not make sufficient taurine since they don't eat meat sources of taurine.  Seaweed is the best vegetarian source of taurine. Vegetarians may not consume sufficient Thiamine since few veggies are good sources.  Whole grains, legumes, and nuts and seeds contain thiamine.  Many of these sources can be hard to digest and absorb for people with Celiac disease.   You may find taking the forms of thiamine called Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) and a B Complex will give the benefits you're looking for better than taurine alone.  
    • knitty kitty
      @Jmartes71, I went to Doterra's site and had a look around.  The Doterra TerraZyme supplement really jumped out at me.  Since we, as Celiacs, often have digestive problems, I looked at the ingredients.  The majority of the enzymes in this supplement are made using black mold, Aspergillus!  Other enzymes are made by yeast Saccharomyces!  Considering the fact that Celiac often have permeable intestines (leaky gut syndrome), I would be very hesitant to take a product like this.  Although there may not be live black mold or yeast in the product, the enzymes may still cause an immune system response which would definitely cause inflammation throughout the body.   Skin, eyes, and intestines are all made from the same basic type of cells.  Your skin on the outside and eyes can reflect how irritated the intestines are on the inside.  Our skin, eyes, and intestines all need the same vitamins and nutrients to be healthy:  Vitamin A, Niacin B3 and Tryptophan, Riboflavin B2, Biotin B7, Vitamin C, and Omega Threes.  Remember that the eight B vitamins work together.  Just taking high doses of just one, vitamin like B12, can cause a deficiency in the others.  Taking high doses of B12 can mask a Folate B9 deficiency.  If you take B12, please take a B Complex, too.  Thiamine B1 can be taken in high doses safely without toxicity.  Thiamine is needed by itself to produce energy so every cell in the body can function, but Thiamine also works with the other B vitamins to make life sustaining enzymes and digestive enzymes.  Deficiencies in either Niacin, Vitamin C, or Thiamine can cause digestive problems resulting in Pellagra, Scurvy, and Gastrointestinal Beriberi.   If you change your diet, you will change your intestinal microbiome.  Following the Autoimmune Protocol Diet, a Paleo diet, will starve out SIBO bacteria.  Thiamine keeps bacteria in check so they don't get out of control as in SIBO.  Thiamine also keeps MOLDS and Yeasts from overgrowth.   Menopause symptoms and menstrual irregularities are symptomatic of low Vitamin D.   Doctors are not as knowledgeable about malnutrition as we need them to be.  A nutritionist or dietician would be more helpful.   Take control of your diet and nutrition.  Quit looking for a pill that's going to make you feel better overnight.  The Celiac journey is a marathon, not a sprint.   "Let food be your medicine, and let medicine be your food."
    • RUKen
      The Lindt (Lindor) dairy-free oat milk truffles are definitely gluten-free, and (last time I checked) so are the white chocolate truffles and the mint chocolate truffles. 
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.