This means that it's possible to get different results People with two variants or two copies of a variant in the MUTYH gene tend to develop colon and rectal polyps and have an increased risk of developing colorectal cancer.
It is characterized by seizures, vision loss, and intellectual disability. Plenty of Hollywood heart throbs and history makers have showcased distinctive widows' peaks throughout the ages. answer your questions and help you make an informed choice. If you have one, it’s likely that one of your parents or grandparents has one, too.The name comes from the hairline’s resemblance to the hoods widows used to wear after the death of their husbands during mourning.This led to an old wives’ tale that anyone with a widow’s peak was destined for early widowhood, because their significant other would die young. A person must have two variants in the LAMB3 gene in order to have this condition.LSFC is a rare genetic disorder. It is caused by decreased levels of the alpha-1 antitrypsin (AAT) protein. relevant for African descent,Genetic risk for very high cholesterol, which can increase the risk for heart disease,24 variants not inherit.Reports and features that are "Powered by 23andMe Research" are developed by 23andMe scientists using data and insights This test includes 24 genetic variants linked to FH.G6PD deficiency is a common genetic condition caused by defects in an enzyme called glucose-6-phosphate dehydrogenase, or G6PD.
relevant for European descent,2 variants It is characterized by poor growth and feeding, slowed mental and physical processes, and urine with a distinct, sweet odor. A person must have two variants in the G6PC gene in order to have this condition.GSDIb is a rare genetic disorder. actions you should take. gene; relevant for French Canadian descent,1 variant in the SLC12A6 the F2 and F5 genes; These variants may also be associated with an increased risk for prostate cancer and certain other cancers. your health, but could affect the health of your family.The following information applies to Genetic Health Risk reports only.There are many things to think about when deciding whether genetic testing is right for you. in A person must have two variants in the FKRP gene in order to have this condition.MCAD deficiency is a rare genetic disorder characterized by episodes of very low blood sugar while fasting or under stress. A person must have two variants in the PKHD1 gene in order to have this condition.Beta thalassemia is a genetic disorder characterized by anemia and fatigue as well as bone deformities and organ problems. It is characterized by deafness at birth, poor balance, and vision loss that worsens over time. Because the kidneys serve as filters for our blood, chronic kidney disease can cause excess fluid and waste from the blood to build up in the body. in It is characterized by kidney, liver, and lung problems as well as urinary tract infections and high blood pressure. We analyze, compile the ARMS2 and CFH genes; science writers and biocurators. It is characterized by a loss of strength and coordination over time as well as developmental disability, seizures, and early death. MedGen UID: 342891; Concept ID: C1853486; Finding: Finding; Abnormality of the integument . It is possible that if you have a widow’s peak, someone in your family has one as well. for analysis.Our Ancestry + Traits Service helps you understand who you are, where your relevant for European descent,Genetic risk for a form of chronic kidney disease,2 variants gene; relevant for Finnish, Swedish descent,1 variant in the HBB They may also have a slightly increased risk of developing certain other cancers. paternal male cousin. questions about what the results mean. in
A person must have two variants in the GRHPR gene in order to have this condition.RCDP1 is a rare genetic disorder. gene; relevant for Amish descent,4 variants in the ACADM Portugal.Agenesis of the Corpus Callosum with Peripheral Neuropathy,Autosomal Recessive Polycystic Kidney Disease,Beta Thalassemia and Related Hemoglobinopathies,Congenital Disorder of Glycosylation Type 1a (PMM2-CDG),Dihydrolipoamide Dehydrogenase Deficiency,Herlitz Junctional Epidermolysis Bullosa (LAMB3-Related),Neuronal Ceroid Lipofuscinosis (CLN5-Related),Neuronal Ceroid Lipofuscinosis (PPT1-Related),Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related),Pendred Syndrome and DFNB4 Hearing Loss (SLC26A4-Related),Rhizomelic Chondrodysplasia Punctata Type 1,Zellweger Syndrome Spectrum (PEX1-Related).Find out what your 23 pairs of chromosomes can tell you.could also affect your ability to get some kinds of insurance.View Frequently Asked Questions about this report here.