invitae nipt gender accuracyinvitae nipt gender accuracy

13Wapner et al. In just over a decade, the tests have gone from laboratory experiments to an industry that serves more than a third of the pregnant women in America, luring major companies like Labcorp and Quest. This is so when you speak to others, they immediately . We did the blood test at 12 weeks. Ive heard 7-10 is average, although it can take longer. Press question mark to learn the rest of the keyboard shortcuts. It's very likely going to be all OK. When are you due? Notice of Data Collection for California Residents, validated in the largest prospective NIPT study ever, the only NIPT that distinguishes the pregnant persons DNA from babys DNA, the approach that creates unique, clinically validated capabilities. Learn more about. My understanding is that its 99% accurate, but that the rare exceptions when its inaccurate can be due to a vanishing twin. The accuracy of the test varies by disorder. You appear to be using incognito/private browsing mode or an ad blocker, which may adversely affect your experience on the site. Published on January 12th, 2021. Invitae NIPT - AVOID . /*# sourceMappingURL=https://www.redditstatic.com/desktop2x/chunkCSS/TopicLinksContainer.3b33fc17a17cec1345d4_.css.map*/Mine was accurate as well. 2022 Jul;227(1):79.e1-79.e11. The presence of medical conditions, like heart defects, can affect the lifespan in these children and adults; however, most individuals with Down syndrome will live into their 60s. Im 37 weeks and Invitae said girl. For Trisomy 18, the negative result accuracy is 97.7 percent, and for Trisomy 13 it's 96.1 percent. Once Invitae receives your sample, on average your healthcare provider will receive the results in: Diagnostic panel testing: 10-21 calendar days. By rejecting non-essential cookies, Reddit may still use certain cookies to ensure the proper functionality of our platform. Non-invasive prenatal screening (NIPS) (also known as NIPT) analyzes cell-free DNA (cfDNA) to assess whether a singleton pregnancy is at increased risk for specific chromosome disorders. Hello! Children with Prader-Willi syndrome have delayed milestones, short stature, rapid weight gain leading to obesity, and intellectual disability. We signed into our results and had them released and it said it we are expecting a girl off of 6% fetal fraction and test taken at 11 weeks. Pregnant with twins? Approximately 1 in 800 biological females will be born with three X chromosomes. 2023 Natera, Inc. All Rights Reserved. 4.3 7 Facts from our Invitae Review Location: San Francisco, CA, USA Products: Sequencing of gene panels and whole exomes (ordered by patients or providers) All Comments (5 . Feb 26, 2023 at 1:17 PM. With my first it said I was having a boy and I did. All medical decisions should be made after discussion with your healthcare provider regarding diagnostic testing during the pregnancy, like chorionic villus sampling (CVS) or amniocentesis, or testing the baby after birth. We have read that you want a higher fetal fraction to make sure it didnt miss the Y chromosome in the blood draw but not sure :/. When we did the ultrasound at the same time the tech said she THINKS its a male but obviously thats just her thought. This is specifically for an actual high risk for ONE of those on the NIPT. And I'm just so frustrated with their process and lack of communication. I got my blood drawn Wednesday 2-22 and got my results early morning Sunday 2-26. You did it! So I had the Invitae nipt test done at the lab at my dr office and the results for the gender said I was having a boy and today I had an ultrasound and the baby is 100% a girl!! Usually its in the 99%. Am J Obstet Gynecol. Im concerned Around 13 weeks I sent in a sample for NIPT testing to Invitae from my doctors office. We respect everyones right to express their thoughts and opinions as long as they remain respectful of other community members, and meet What to Expects Terms of Use. Ive had 3 ultrasounds since that have also shown a girl. Non-invasive prenatal screening is done using a simple blood draw and checks to see the possibility of your baby being affected by certain chromosome conditions, including Down Syndrome. *Certain screening options are only available for singleton pregnancies. We just got our Invitae NIPT results that says the predicted sex is female. Please whitelist our site to get all the best deals and offers from our partners. Prader-Willi syndrome occurs when either a small piece of chromosome 15 is missing or when both copies of chromosome 15 come from the same parent (called uniparental disomy, or UPD). Create an account to follow your favorite communities and start taking part in conversations. No use of any Invitae trademark, trade name, or trade dress in this website may be made without the prior written authorization of Invitae, except to identify Invitaes products or services. Jun 21, 2021 at 11:10 AM. 2016;18(10):1056-1065. It can detect multiples because it analyses chromosomal material and can identify and differentiate between individuals in this way. Invitaes mission is to bring comprehensive genetic information into mainstream medicine to improve healthcare for billions of people. Invitae is a clinical genetic testing company that focuses on health screenings. NIPT checks for the presence or absence of the Y chromosome in the fetus and estimates how many are present. ._1sDtEhccxFpHDn2RUhxmSq{font-family:Noto Sans,Arial,sans-serif;font-size:14px;font-weight:400;line-height:18px;display:-ms-flexbox;display:flex;-ms-flex-flow:row nowrap;flex-flow:row nowrap}._1d4NeAxWOiy0JPz7aXRI64{color:var(--newCommunityTheme-metaText)}.icon._3tMM22A0evCEmrIk-8z4zO{margin:-2px 8px 0 0} Since my anatomy scan Ive been googling like crazy and have officially drained myself by crying and freaking out over the possibility of anything being wrong with her heart/Down syndrome (my husband and I spoke previously I would terminate if chromosomal abnormalities were there). Feb 24, 2023 at 4:02 PM. my FF was 3.0% and correct so yes. This educational content is not medical or diagnostic advice. and they say that the results are 99.9% and the gender is more accurate than the results at the atonamy scan. ._2cHgYGbfV9EZMSThqLt2tx{margin-bottom:16px;border-radius:4px}._3Q7WCNdCi77r0_CKPoDSFY{width:75%;height:24px}._2wgLWvNKnhoJX3DUVT_3F-,._3Q7WCNdCi77r0_CKPoDSFY{background:var(--newCommunityTheme-field);background-size:200%;margin-bottom:16px;border-radius:4px}._2wgLWvNKnhoJX3DUVT_3F-{width:100%;height:46px} This test has been validated on full region deletions of Prader-Willi syndrome/Angelman syndrome (PWS/AS) only and might be unable to detect smaller deletions. This educational content is not medical or diagnostic advice. My husband is calm and told me if doctors arent worried, he isnt, and that the NIPT is all we need to know baby girl is healthy. Does anyone know the accuracy of the Panorama blood test for gender? We strive to provide you with a high quality community experience. Introducing MaterniT21 PLUS with GENOME-Flex. 1. My NIPT test was done a month or two ago, and everything came back negative for abnormalities. 2014. Non-invasive prenatal screening (NIPS) is another important part of a healthy pregnancyplus it can predict your babys sex as early as 10 weeks. NIPT is beginning to be used to test for genetic disorders that are caused by changes (variants) in single genes. It is extremely rare for these pregnancies to reach term as they typically spontaneously miscarry early in pregnancy. Mine was 6% and said we were having a boy confirmed by ultrasound multiple times. The views expressed in community are solely the opinions of participants, and do not reflect those of What to Expect. Validated in SMART, the largest prospective NIPT study with over 20,000 participants enrolled. These conditions are due to extra or missing genetic material called chromosomes, which may lead to a medical condition. About 1 in 5,000 newborn babies has 1p36 deletion syndrome. Look at your report and what they report to be PPV or NPV. I'm lab technologist. ._2ik4YxCeEmPotQkDrf9tT5{width:100%}._1DR1r7cWVoK2RVj_pKKyPF,._2ik4YxCeEmPotQkDrf9tT5{display:-ms-flexbox;display:flex;-ms-flex-align:center;align-items:center}._1DR1r7cWVoK2RVj_pKKyPF{-ms-flex-pack:center;justify-content:center;max-width:100%}._1CVe5UNoFFPNZQdcj1E7qb{-ms-flex-negative:0;flex-shrink:0;margin-right:4px}._2UOVKq8AASb4UjcU1wrCil{height:28px;width:28px;margin-top:6px}.FB0XngPKpgt3Ui354TbYQ{display:-ms-flexbox;display:flex;-ms-flex-align:start;align-items:flex-start;-ms-flex-direction:column;flex-direction:column;margin-left:8px;min-width:0}._3tIyrJzJQoNhuwDSYG5PGy{display:-ms-flexbox;display:flex;-ms-flex-align:center;align-items:center;width:100%}.TIveY2GD5UQpMI7hBO69I{font-size:12px;font-weight:500;line-height:16px;color:var(--newRedditTheme-titleText);white-space:nowrap;overflow:hidden;text-overflow:ellipsis}.e9ybGKB-qvCqbOOAHfFpF{display:-ms-flexbox;display:flex;-ms-flex-align:center;align-items:center;width:100%;max-width:100%;margin-top:2px}.y3jF8D--GYQUXbjpSOL5.y3jF8D--GYQUXbjpSOL5{font-weight:400;box-sizing:border-box}._28u73JpPTG4y_Vu5Qute7n{margin-left:4px} 8Nicolaides et al. If born alive, most affected babies with trisomy 13 will pass away within the first few weeks of life. However, you cannot know for sure if your baby has that condition based upon the screening result alone. If this is the case, trisomies 21, 18 and 13, and fetal sex (optional) will be screened using Vasistera NIPT and will be reported separately. Approximately 1 in 1,000 biological males will be born with one X chromosome and two Y chromosomes. In rare instances, triploid pregnancies can persist and progress to a type of cancer called choriocarcinoma. Fast turnaround. Others, such as microdeletions, occur when a chromosome is missing a small piece of genetic information.1. Thank god everything came back negative! In most cases, babies with monosomy X will need extra medical care including hormone therapyat various stages of life. Hello! Testing can also predict your babys sex (if youd like to know). What to Expect supports Group Black and its mission to increase greater diversity in media voices and media ownership. For example, when testing for Trisomy 21 (Down Syndrome), the negative result accuracy of the test is 99.5 percent. 10Martin et al. CAP accredited, ISO 13485 certified, and CLIA certified. About 10 percent survive to their first birthday. This educational content is not medical or diagnostic advice. They may also have growth delays, behavior problems, and some have curvature of the spine (scoliosis). I am having a girl took invitae nipt at 14 weeks with 20% fetal fraction still accurate for me. Please specify a reason for deleting this reply from the community. Miscarriage occurs in about 30% of pregnancies with Down syndrome while overall about 1 in 700 babies are born with Down syndrome. Genetic information is important for every pregnancy. This time it says its a girl so it better be accurate or I will cry for days. I used Invitae last year and it was accurate. It's mainly used to screen for Down's Syndrome and two other. Babies with Prader-Willi syndrome have low muscle tone and problems with growth and feeding. The name Cri-du-chat was given to this syndrome due to the high-pitched, cat-like cry that babies with this syndrome often make. It came back and said predicted sex: male. It says 99%, but Ive read other places 99.9either way, super accurate! For more information, please see our Anatomy scan confirmed its a girl. An important part of pregnancy care. I just got my blood work done around noon and just before the company picks up the samples so I'm hoping I'll have them sooner than later. It's very rare for these tests to be wrong. Non-invasive prenatal screening is done using a simple blood draw and checks to see the possibility of your baby being affected by certain chromosome conditions, including Down Syndrome. Group Black's collective includes Essence, The Shade Room and Naturally Curly. All rights reserved. Invitae NIPTs gender accuracy? Because fetal aneuploidy can affect any pregnancy, all pregnant women should be offered screening. About one in every 20,000 babies is born with Cri-du-chat syndrome. The majority of children with this disorder have heart defects, immune system problems, and specific facial features. Test code: 71005 5-7 calendar days. 2013 June;33(6):575-9. Just wanted to hear from you all about the test accuracy. Please disable any ad blockers and view the site in non-private mode. Thank you so much! Screening for fetal chromosomal abnormalities. Please specify a reason for deleting this reply from the community. Got my gender results through Invitae 3 weeks ago and its 99.9% accurate!! What to Expect supports Group Black and its mission to increase greater diversity in media voices and media ownership. ?Due April 30 with a baby girl! They told me everything else appeared normal but they couldnt get clear shots of her spine so were going back in 5 weeks, where they also will be checking her heart again for my peace of mind. Fetal fraction 9 percent. From prenatal vitamins to prenatal yoga, youre doing everything you can to ensure your baby is healthy. Designed by Elegant Themes | Powered by WordPress. *SNP, single nucleotide polymorphism, Panorama evaluates SNPs the 1% of our DNA that makes us different from one another. my results came back inconclusive and there is a fine print that says it's only 50% accurate. I'll have a confirmation US at 20 weeks next month :) Having a girl! Its tests can be more expensive than competitor products. Limited Noninvasive Prenatal Testing (NIPT), Schedule Session with Patient Coordinator, Order Tests and Track Status on NateraConnect. /*# sourceMappingURL=https://www.redditstatic.com/desktop2x/chunkCSS/IdCard.ea0ac1df4e6491a16d39_.css.map*/._2JU2WQDzn5pAlpxqChbxr7{height:16px;margin-right:8px;width:16px}._3E45je-29yDjfFqFcLCXyH{margin-top:16px}._13YtS_rCnVZG1ns2xaCalg{font-family:Noto Sans,Arial,sans-serif;font-size:14px;font-weight:400;line-height:18px;display:-ms-flexbox;display:flex}._1m5fPZN4q3vKVg9SgU43u2{margin-top:12px}._17A-IdW3j1_fI_pN-8tMV-{display:inline-block;margin-bottom:8px;margin-right:5px}._5MIPBF8A9vXwwXFumpGqY{border-radius:20px;font-size:12px;font-weight:500;letter-spacing:0;line-height:16px;padding:3px 10px;text-transform:none}._5MIPBF8A9vXwwXFumpGqY:focus{outline:unset} Authors: Peer Dar, MD | Bo Jacobsson, MD, PhD | Rebecca Clifton, PhD | Charlly Kao, PhD | Hakon Hakonarson, MD, PhD | Mary E. Norton, MD, Authors: Peer Dar, MD | Bo Jacobsson, MD, PhD | Cora MacPherson, PhD | Charlly Kao, PhD | Hakon Hakonarson, MD, PhD | Mary E. Norton, MD, Panorama screens for common genetic conditions that are caused by extra or missing chromosomes in the babys DNA. For example, when Panorama shows a high risk result for Trisomy 21, there is a 95% chance that the fetus is affected by Trisomy 21. Assuming 50 pregnant women are tested every year, 21 of these will avoid invasive testing. I've never in my life heard a story of it being wrong and I my self work with blood. nipt says boy ultrasound says girl. I would also like to know because my ultrasound said I was due in May and invitae says Im due in March. Please select a reason for escalating this post to the WTE moderators: Connect with our community members by starting a discussion. J Clin Med. p.s. The educational health content on What To Expect is reviewed by our medical review board and team of experts to be up-to-date and in line with the latest evidence-based medical information and accepted health guidelines, including the medically reviewed What to Expect books by Heidi Murkoff. The educational health content on What To Expect is reviewed by our medical review board and team of experts to be up-to-date and in line with the latest evidence-based medical information and accepted health guidelines, including the medically reviewed What to Expect books by Heidi Murkoff. 6Pergament et al. Is this pretty accurate? More than 3 million people in more than 60 countries have chosen Panorama for genetic testing during pregnancy. **10 Group Owners uphold the core values of the brand by reporting content that violates the community guidelines. Group Black's collective includes Essence, The Shade Room and Naturally Curly. .ehsOqYO6dxn_Pf9Dzwu37{margin-top:0;overflow:visible}._2pFdCpgBihIaYh9DSMWBIu{height:24px}._2pFdCpgBihIaYh9DSMWBIu.uMPgOFYlCc5uvpa2Lbteu{border-radius:2px}._2pFdCpgBihIaYh9DSMWBIu.uMPgOFYlCc5uvpa2Lbteu:focus,._2pFdCpgBihIaYh9DSMWBIu.uMPgOFYlCc5uvpa2Lbteu:hover{background-color:var(--newRedditTheme-navIconFaded10);outline:none}._38GxRFSqSC-Z2VLi5Xzkjy{color:var(--newCommunityTheme-actionIcon)}._2DO72U0b_6CUw3msKGrnnT{border-top:none;color:var(--newCommunityTheme-metaText);cursor:pointer;padding:8px 16px 8px 8px;text-transform:none}._2DO72U0b_6CUw3msKGrnnT:hover{background-color:#0079d3;border:none;color:var(--newCommunityTheme-body);fill:var(--newCommunityTheme-body)} mine does not say that anywhere so this is helpful to know, thank you. I'm lab technologist. A Group Leader is a What to Expect community member who has been selected by our staff to help maintain a positive, supportive tone within a group. 35;(3):212-7. We are having our second baby boy :) Even though they posted about longer lab processing times, invitae was twice as fast as myriad which I used with my first pregnancy. Trisomy 18 occurs in approximately 1 in 3,000 live births. 7Ryan et al. What to Expect supports Group Black and its mission to increase greater diversity in media voices and media ownership. Deep breaths. Children with Down syndrome will need extra medical care depending on the childs specific health problems. Group Owners uphold the core values of the brand by reporting content that violates the community guidelines. ._3bX7W3J0lU78fp7cayvNxx{max-width:208px;text-align:center} It was released to me today. We respect everyones right to express their thoughts and opinions as long as they remain respectful of other community members, and meet What to Expects Terms of Use. Want to start the conversation with your doctor? nipt results came back and still boy. Visible abnormalities include extra fingers and/or toes or an opening in the lip, with or without an opening in the palate. Most children with 22q.11.2 deletion syndrome have mild-to-moderate intellectual disability and speech delays; some will also have low calcium levels, kidney problems, feeding problems, and/or seizures. Anyone know how accurate testing can be for the had a gender reveal party with sneakpeak results and I was a little nervous about accuracy of the at home test but went with it anyways. my fetal traction was only 4.3% does that make it any less accurate? Pretty good odds for accuracy. Post your pictures. ._9ZuQyDXhFth1qKJF4KNm8{padding:12px 12px 40px}._2iNJX36LR2tMHx_unzEkVM,._1JmnMJclrTwTPpAip5U_Hm{font-size:16px;font-weight:500;line-height:20px;color:var(--newCommunityTheme-bodyText);margin-bottom:40px;padding-top:4px;text-align:left;margin-right:28px}._2iNJX36LR2tMHx_unzEkVM{-ms-flex-align:center;align-items:center;display:-ms-flexbox;display:flex}._2iNJX36LR2tMHx_unzEkVM ._24r4TaTKqNLBGA3VgswFrN{margin-left:6px}._306gA2lxjCHX44ssikUp3O{margin-bottom:32px}._1Omf6afKRpv3RKNCWjIyJ4{font-size:18px;font-weight:500;line-height:22px;border-bottom:2px solid var(--newCommunityTheme-line);color:var(--newCommunityTheme-bodyText);margin-bottom:8px;padding-bottom:8px}._2Ss7VGMX-UPKt9NhFRtgTz{margin-bottom:24px}._3vWu4F9B4X4Yc-Gm86-FMP{border-bottom:1px solid var(--newCommunityTheme-line);margin-bottom:8px;padding-bottom:2px}._3vWu4F9B4X4Yc-Gm86-FMP:last-of-type{border-bottom-width:0}._2qAEe8HGjtHsuKsHqNCa9u{font-size:14px;font-weight:500;line-height:18px;color:var(--newCommunityTheme-bodyText);padding-bottom:8px;padding-top:8px}.c5RWd-O3CYE-XSLdTyjtI{padding:8px 0}._3whORKuQps-WQpSceAyHuF{font-size:12px;font-weight:400;line-height:16px;color:var(--newCommunityTheme-actionIcon);margin-bottom:8px}._1Qk-ka6_CJz1fU3OUfeznu{margin-bottom:8px}._3ds8Wk2l32hr3hLddQshhG{font-weight:500}._1h0r6vtgOzgWtu-GNBO6Yb,._3ds8Wk2l32hr3hLddQshhG{font-size:12px;line-height:16px;color:var(--newCommunityTheme-actionIcon)}._1h0r6vtgOzgWtu-GNBO6Yb{font-weight:400}.horIoLCod23xkzt7MmTpC{font-size:12px;font-weight:400;line-height:16px;color:#ea0027}._33Iw1wpNZ-uhC05tWsB9xi{margin-top:24px}._2M7LQbQxH40ingJ9h9RslL{font-size:12px;font-weight:400;line-height:16px;color:var(--newCommunityTheme-actionIcon);margin-bottom:8px} Please select a reason for escalating this post to the WTE moderators: Connect with our community members by starting a discussion. If you feel a message or content violates these standards and would like to request its removal please submit the following information and our moderating team will respond shortly. Ultrasounds on the other hand. Reddit and its partners use cookies and similar technologies to provide you with a better experience. Babies with triploidy have a complete extra set of chromosomes for a total of 69 chromosomes instead of the usual 46. 2Dar et al. A Group Leader is a What to Expect community member who has been selected by our staff to help maintain a positive, supportive tone within a group. 27 febrero, 2023 . If you feel a message or content violates these standards and would like to request its removal please submit the following information and our moderating team will respond shortly. About 1 in 500 biological males will be born with Klinefelter syndrome. what happens if you forgot to put unemployment on taxes, Non-invasive prenatal screening (NIPS) | Test Invitae, How accurate are Invitae results? NIPT has been available privately in the UK since 2012 and is available to any woman or couple who want to pay the bill of up to 500. A place for Canadian redditors, those who want to have children, are having children, have children, and anyone who supports them. I found out babys gender through NIPT testing and everything else came back as healthy baby! So I think 6% is a good fetal fraction! Clin Genet. Read the pdf they send you there's more info. Baby!!!!!!!!!!!!!!!! Use of this site is subject to our terms of use and privacy policy. Yesterday was my anatomy scan, where they told me baby has an EIF on her heart (bright spot and soft marker for Down syndrome). They often have birth defects involving the heart, brain, and kidneys. Prenat Diagn. PPV for 22q11.2 deletion syndrome and Angelman syndrome in published studies was 53% and 10% respectively when no ultrasound anomalies were seen and was up to 100% when ultrasound anomalies were seen prior to testing. *1,5-7; Panorama is the only test that differentiates between pregnant person's and fetal DNA, which helps avoid false positives and false negatives. Panorama can be performed as early as nine weeks gestation. Obstet Gynecol. A missing piece of chromosome 5 causes Cri-du-chat syndrome, also called 5p- (5p minus) syndrome. You can't eliminate uncertainty in pregnancy, but with NIPS & carrier screening you can get closer. Apr 20, 2022 at 7:04 PM. Unless otherwise specified, all product names, service names, and logos appearing in this website are trademarks owned by or licensed to Invitae, its subsidiaries, or its affiliates. Gregg AR, Skotko BG, Benkendorf JL et al. Invitae's next-generation sequencing approach for evaluating exons 12-15 of PMS2 is a two-step process for sequence variants and a three-step process for intragenic deletions and duplications. For Prader-Willi syndrome, no risk assessment is reported at FF 2.8%. Group Leaders arent expected to spend any additional time in the community, and are not held to a set schedule. What Is the Baking Soda Gender Test and Does It Really Work? they wouldn't have released results unless they were certain. ._3-SW6hQX6gXK9G4FM74obr{display:inline-block;vertical-align:text-bottom;width:16px;height:16px;font-size:16px;line-height:16px} So that's a 4 in 1,000 chance of either being wrong, or that you couldn't get a result because there wasn't enough material (often because done closer to 10wks). For example, in a group of Trisomy 21 cases, Panorama will correctly identify more than 99% of those cases. Testing in 7th gestational week or later provides more reliable results than testing before week 7. So anyway, stay away! b. babybeard618. The tests described have been developed and their performance characteristics determined by the CLIA-certified laboratory performing the test. Group Leaders arent expected to spend any additional time in the community, and are not held to a set schedule. e. Feb 24, 2023 at 4:00 PM. 1ACOG Practice Bulletin 226. Dont want to start buying items and Genetic testing said were both carriers for CF. If born alive, most affected babies with trisomy 18 will pass away within the first few weeks of life. The at home kits can mistakenly tell you girl if there isn't enough fetal DNA to actually notice the chromosone. Babies with trisomy 13 have three copies of chromosome 13 and have severe intellectual disabilities. For more details, please see the resources section below. Group Black's collective includes Essence, The Shade Room and Naturally Curly. Panorama can be performed as early as nine weeks . 2023 Invitae Corporation. I worried about the same thing but my midwife assured me that if they didnt have sufficient FF to get accurate results it wouldve just came back inconclusive. ._3Qx5bBCG_O8wVZee9J-KyJ{border-top:1px solid var(--newCommunityTheme-widgetColors-lineColor);margin-top:16px;padding-top:16px}._3Qx5bBCG_O8wVZee9J-KyJ ._2NbKFI9n3wPM76pgfAPEsN{margin:0;padding:0}._3Qx5bBCG_O8wVZee9J-KyJ ._2NbKFI9n3wPM76pgfAPEsN ._2btz68cXFBI3RWcfSNwbmJ{font-family:Noto Sans,Arial,sans-serif;font-size:14px;font-weight:400;line-height:21px;display:-ms-flexbox;display:flex;-ms-flex-pack:justify;justify-content:space-between;-ms-flex-align:center;align-items:center;margin:8px 0}._3Qx5bBCG_O8wVZee9J-KyJ ._2NbKFI9n3wPM76pgfAPEsN ._2btz68cXFBI3RWcfSNwbmJ.QgBK4ECuqpeR2umRjYcP2{opacity:.4}._3Qx5bBCG_O8wVZee9J-KyJ ._2NbKFI9n3wPM76pgfAPEsN ._2btz68cXFBI3RWcfSNwbmJ label{font-size:12px;font-weight:500;line-height:16px;display:-ms-flexbox;display:flex;-ms-flex-align:center;align-items:center}._3Qx5bBCG_O8wVZee9J-KyJ ._2NbKFI9n3wPM76pgfAPEsN ._2btz68cXFBI3RWcfSNwbmJ label svg{fill:currentColor;height:20px;margin-right:4px;width:20px;-ms-flex:0 0 auto;flex:0 0 auto}._3Qx5bBCG_O8wVZee9J-KyJ ._4OtOUaGIjjp2cNJMUxme_{-ms-flex-pack:justify;justify-content:space-between}._3Qx5bBCG_O8wVZee9J-KyJ ._4OtOUaGIjjp2cNJMUxme_ svg{display:inline-block;height:12px;width:12px}._2b2iJtPCDQ6eKanYDf3Jho{-ms-flex:0 0 auto;flex:0 0 auto}._4OtOUaGIjjp2cNJMUxme_{padding:0 12px}._1ra1vBLrjtHjhYDZ_gOy8F{font-family:Noto Sans,Arial,sans-serif;font-size:12px;letter-spacing:unset;line-height:16px;text-transform:unset;--textColor:var(--newCommunityTheme-widgetColors-sidebarWidgetTextColor);--textColorHover:var(--newCommunityTheme-widgetColors-sidebarWidgetTextColorShaded80);font-size:10px;font-weight:700;letter-spacing:.5px;line-height:12px;text-transform:uppercase;color:var(--textColor);fill:var(--textColor);opacity:1}._1ra1vBLrjtHjhYDZ_gOy8F._2UlgIO1LIFVpT30ItAtPfb{--textColor:var(--newRedditTheme-widgetColors-sidebarWidgetTextColor);--textColorHover:var(--newRedditTheme-widgetColors-sidebarWidgetTextColorShaded80)}._1ra1vBLrjtHjhYDZ_gOy8F:active,._1ra1vBLrjtHjhYDZ_gOy8F:hover{color:var(--textColorHover);fill:var(--textColorHover)}._1ra1vBLrjtHjhYDZ_gOy8F:disabled,._1ra1vBLrjtHjhYDZ_gOy8F[data-disabled],._1ra1vBLrjtHjhYDZ_gOy8F[disabled]{opacity:.5;cursor:not-allowed}._3a4fkgD25f5G-b0Y8wVIBe{margin-right:8px} Intellectual disabilities places 99.9either way, super accurate!!!!!... 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