the purpose of reporting and interpreting genetic health risks and reporting carrier status. the MUTYH gene; relevant for European descent, Genetic risk for a form of chronic kidney disease, 2 variants One full-priced kit must be purchased for subsequent kits of the same service type professional before making any major lifestyle changes. Hereditary thrombophilia is a predisposition to developing harmful blood clots. Limit 10 include both reports that meet FDA requirements for genetic health risks and the 23andMe Type 2 Diabetes health individually validated for accuracy. Type 2 Diabetes Customer Reviews. in Trace DNA through your close family and explore the genetic gene; relevant for Irish, Northern European descent, 1 variant in the SLC17A5 Finnish, French & German, Greek & Balkan, Italian, Sardinian, Scandinavian, Spanish & Portuguese); 23andMe was founded in 2006 to help people access, understand and benefit from the human genome. Celiac Disease, gene; relevant for French Canadian descent, 1 variant in the SLC12A6 These reports do not include variants in other genes linked to hereditary cancers and the absence of variants included in these reports do not rule out the presence of other genetic variants that may impact cancer risk. near relevant for Northern European descent, Genetic risk for a form of movement impairment, 2 variants variant found and studied in many ethnicities, Genetic risk for a specific colorectal cancer syndrome, 2 variants Health predisposition reports include both reports that meet FDA requirements for genetic health risks and the 23andMe Type 2 Diabetes health predisposition report which is based on 23andMe research and … in Find and connect with relatives in the 23andMe database who share DNA with you. the SERPINA1 gene; gene; relevant for African American, African, Middle Eastern, South Asian, Caribbean, Mediterranean, Central and South American descent, 1 variant in the ALDH3A2 the G6PD gene; The PGS test is not a substitute for visits to a healthcare professional for recommended screenings or appropriate follow-up. gene; relevant for Amish descent, 4 variants in the ACADM Consult with a healthcare relevant for African, Southern European, Kurdish Jewish, Middle Eastern, Central Asian, South Asian descent, Genetic risk for a form of nerve and heart damage, 3 variants Customer Reviews ... Canada United Kingdom International Europe Denmark (EN) Finland (EN) Ireland Read more. predisposition report which is based on 23andMe research and has not been reviewed by FDA. 23andme.com/test-info/. qualitative genotyping to detect select clinically relevant variants in the genomic DNA of adults from saliva for Read more. gene; relevant for French Canadian, Finnish descent, 1 variant in the PCDH15 online, from anywhere. Discount applied on each additional kit of the same service Read more. gene; relevant for European descent, 1 variant in the LRPPRC gene; relevant for Ashkenazi Jewish descent, *The 23andMe PGS test includes health predisposition and carrier status reports. These carrier reports are not intended to tell you anything about type that is purchased in the same order and shipped to a single address. gene; relevant for Ashkenazi Jewish descent, 3 variants in the ASPA Reports included: higher risk of developing a disease, but does not describe a person’s overall risk of developing the disease. to receive the discount. to receive the discount. gene; relevant for Ashkenazi Jewish descent, 1 variant in the CLRN1 only for informational use and not for medical, diagnostic or other use. See the list of important policies below. Research higher risk of developing a disease, but does not describe a person’s overall risk of developing the disease. ). We have more than three million genotyped customers around the world. Enter a few pieces of information. Results should be confirmed in a clinical setting before taking any medical action. 23andMe was founded in 2006 to help people access, understand and benefit from the human genome. Warnings & Limitations: The 23andMe PGS Genetic Health Risk Report for BRCA1/BRCA2 (Selected Variants) is indicated for reporting of the 185delAG and 5382insC variants in the BRCA1 gene and the 6174delT variant in the BRCA2 gene. Chinese Dai, Filipino & Austronesian, Indonesian, Thai, Khmer & Myanma, Japanese, Korean, Manchurian or small. This report does not include variants in other genes linked to hereditary cancers and the absence of variants included in this report does not rule out the presence of other genetic variants that may impact cancer risk. ), Enter your email to unlock the best offer of the year, *Entry of your email address is not necessary to redeem the. the BRCA1 and BRCA2 genes; See how many Neanderthal variants you have, how that compares to others and what it means for you. Discount not applicable to Reports and features that are "Powered by 23andMe Research" are developed by 23andMe scientists using data and insights Cannot be combined or used in conjunction with any other gene; relevant for Finnish descent, 3 variants in the SMPD1 you could pay as low as $33.17/month for 6 months at 0% APR.). (or please visit 23andMe's International site. Start a family tree automatically based on your DNA. Your ethnicity may affect the relevance of each report and how your genetic health risk Changing your location to a region outside the EU may impact how your information is processed. BRCA1/BRCA2 (Selected Variants), Lactose Intolerance, The ** If your country is not listed, please visit the International site. gene; relevant for Ashkenazi Jewish descent, 3 variants in the ABCC8 The test uses gene; relevant for Ashkenazi Jewish descent, 2 variants in the PMM2 granular view of your ancestry, plus immersive educational content. The PGS test is not a substitute for visits to a healthcare professional for recommended screenings or appropriate follow-up. Keep in mind EU data protection laws may no longer apply. gene; relevant for Sardinian, Cypriot, Italian/Sicilian, Greek descent, 1 variant in the BLM Health predisposition reports Egyptian, Cypriot, Egyptian, Iranian, Caucasian & Mesopotamian, Levantine, North African, Peninsular Arab), Genetic likelihood for a disorder of blood sugar regulation, 1,000+ variants in many genes; variants found in many ethnicities, Genetic risk for a form of adult-onset vision loss, 2 variants report, visit We have more than three million genotyped customers around the world. diagnose any disease. gene; relevant for Ashkenazi Jewish descent, 1 variant in the G6PC 23andMe was founded in 2006 to help people access, understand Each genetic health risk report describes if a person has variants associated with a gene; relevant for Ashkenazi Jewish, European descent, 23 variants in the PAH 30+ traits including: determine any treatment. kits of the same service type may receive the discount. 10+ reports including: We are here to help with your questions. We have more than three million genotyped customers around the world. Malayali Subgroup, Northern Indian & Pakistani, Southern Indian & Sri Lankan, Southern Indian Subgroup); Stay in the know about all things 23andMe. No question is too big Learn the origins of your maternal and paternal ancestors and where they lived thousands The report describes if a woman is at increased risk of developing breast and ovarian cancer, and if a man is at increased risk of developing breast cancer or may be at increased risk of developing prostate cancer. It is not intended to and benefit from the human genome. Type 2 Diabetes Each genetic health risk report describes if a person has variants associated with a Late-Onset Alzheimer's Disease, See what customers are saying about us. results are interpreted. (, 40+ reports including: in gene; relevant for Ashkenazi Jewish descent, 7 variants in the MEFV gene; relevant for Ashkenazi Jewish descent, 1 variant in the MCOLN1 For important information and limitations regarding each genetic health risk and carrier status developing a particular disease later in life. Read more. Read more. relevant for African descent, Genetic risk for very high cholesterol, which can increase the risk for heart disease, 24 variants See what customers are saying about us. You can make a difference by participating in research — in the LDLR and APOB genes; not inherit. determine any treatment. Read more. Our carrier status reports can be used to determine carrier status, but cannot determine Divide your purchase into 6 equal monthly payments. Blog. your risk for developing a disease in the future, the health of your fetus, or your newborn child's risk of Americas (Caribbean, Mexico & Central America, Native American, South America); East Asia (Chinese, Changing your location to a region outside the EU may impact how your information is processed. **This data has undergone a general quality review however only a subset of markers have been the APOE gene; Read more. Read more. Male Bald Spot, Read more. Read more. (or please visit 23andMe's International site. the TTR gene; Limit 10 gene; relevant for European descent, 2 variants in the BCKDHB