Genomic Testing for Genetic SNPs (Single Nucleotide Pleomorphisms) can be identified through a simple saliva swab. These characteristics provide valuable information about how an individual processes vitamins and minerals, glucose and hormones as well as reveal familial genes governing metabolism and memory and cognitive health. If you have a family history of conditions such as breast cancer, diabetes, Alzheimer’s (type III diabetes), dementia or Parkinson’s Disease, genetic testing can reveal your potential tendency toward developing the condition. If a SNP is present you can supplement with targeted nutrients to minimize those deficits. Weight management is another area which SNPs, once identified, can help.
Genomic testing can put your mind at ease or arm you with the information to supply specific nutrients to counterbalance the metabolic deficiency. Especially in cases of adopted children who are unaware of their biological parents’ physical status, genomic testing can be a valuable tool. There’s an important connection between our genes, nutrition and health.
Nutrigenomics takes what we know from nutritional science and genetics, then reveals how it all works together to shape your health.
Send us your 23andMe report via email and schedule your genomic analysis. We translate your genetic data from genomic testing — previously collected by 23andMe® or Ancestry® — into easy-to-interpret reports that identify more than 70 scientifically credible genetic variations, called single nucleotide polymorphisms (SNPs), and their eleven associated trait categories that can affect your health. Using these findings, our reports provide easy-to-understand nutritional and lifestyle recommendations that are tailored to your unique genetic needs. As additional clinically relevant SNPs are discovered, our reports are automatically updated.
Your practical lifestyle and nutritional recommendations are rooted in science and medical research, and geared toward helping you achieve optimal health
From a homeopathic perspective, you might also consider the concept of miasms. See our page on Homeopathy.
Email us at: email@example.com
Also see the Center for Homeopathy on inherited characteristics.
Visit the CDC website to learn more about genomic testing.
If you have someone in your family who had or has cancer, genomic testing might give you information to derail potential disease processes.
For example, see Cancer Connect’s website.
The information below is from the Dana Farber Cancer Prevention Center. Visit their website for further details.
Genetic and genomic testing enables the examination of DNA and assists in determining susceptibility to inherited diseases. Genetic testing for cancer predisposition has traditionally been done by looking at one gene at a time. With advances in technology, multiple genes can be evaluated in parallel through one test — this is referred to as panel testing or multiplex testing. New technologies such as whole genome or exome testing (evaluation of the complete set of DNA) of a person or a tumor may identify hereditary cancer predisposition.
Our Specialty Centers and Programs
Clinicians in our specialty centers and programs provide state-of-the-art care, while helping patients and families to understand their cancer risk and suggest ways to lower risk.
We partner with medical oncologists and gynecological oncology surgeons, geneticists, and genetic counselors to evaluate your personal or family history of breast and ovarian cancers and other associated cancers. Patients learn what steps they can take to reduce their risk of developing breast and ovarian cancer.
Colorectal cancer can run in families, and about 5 to 10 percent of colorectal cancer is thought to be hereditary. We offer advanced genetic testing to determine an individual’s risk for colorectal cancer. Our practice follows patients who have an increased risk for polyps, colorectal cancers, gastrointestinal cancers, Lynch syndrome, and related cancers. We also offer risk assessment and genetic testing for individuals who may be at increased risk for pancreatic cancer and determine eligibility for screening studies.
Lynch syndrome is a genetic condition that increases the risk of certain cancers. The Lynch Syndrome Center is the largest and most comprehensive multidisciplinary cancer genetics group in the region that specializes in coordinating the care of people with Lynch syndrome. The Center’s mission is to provide personalized and comprehensive preventive care and treatment for families with Lynch syndrome, supported by world class research and state-of-the-art diagnostics. Our specialists act as quarterbacks, by creating personalized management plans for people who have Lynch syndrome. Lynch syndrome is a multi-organ disease associated with colon, uterine, and pancreatic cancer among others, and we ensure careful monitoring and managing the disease to prevent each of these cancers in our patients.
Dana-Farber’s Li-Fraumeni Syndrome and TP53 Center is the first comprehensive multi-disciplinary center in the world that specializes in coordinating the care of people with LFS and TP53+ results, as well as provides psychological and social support for patients and their families. Our team of internationally renowned experts develops personalized cancer risk management plans for children, adolescents, and adults with LFS and TP53+ results, and will work with their health care providers – oncologists, pediatricians, primary care physicians, and others – to provide ongoing care.
Hereditary Paraganglioma-Pheochromocytoma Syndrome (PGL/PCC)
The Paraganglioma-Pheochromocytoma Genetics Group is a collaborative initiative of Dana-Farber’s Cancer Genetics and Prevention Program and Brigham and Women’s Endocrine Division – with endocrinologists, geneticists, oncologists, and genetic counselors dedicated to providing patients with personalized hereditary risk evaluation, genetic testing, recommendations for screening and prevention, and long-term follow-up.
Gastrointestinal Stromal Tumors (GIST)
By looking at the genes of people with GIST, we have learned about inherited forms of GIST and how best to monitor individuals at high genetic risk.
Learn more about GIST
Testing for Syndromes and Genes
Some of the testing capabilities at Dana-Farber Cancer Institute include:
- Hereditary Breast and/or Ovarian Cancer: BRCA1, BRCA2, PALB2, CHEK2, BRIP1, NBN, RAD50, RAD51C, RAD51D, ATM, BARD1
- Li-Fraumeni Syndrome: TP53
- Lynch Syndrome or Hereditary Nonpolyposis Colorectal Cancer: MLH1, MSH2, MSH6, PMS2, EPCAM
- Familial Adenomatous Polyposis (FAP) and Attenuated Familial Adenomatous Polyposis: APC, MUTYH
- Familial Pancreatic Cancer: BRCA2, BRCA1, STK11, CDKN2A, MLH1, MSH2, MSH6, PMS2, EPCAM
- Paraganglioma and Pheochromocytoma Syndrome: SDHB, SDHD, SDHC, SDHA, SDHAF2, TMEM127, MAX, NF1, FH, RET, VHL
- Cowden Syndrome: PTEN
- Multiple Endocrine Neoplasia Type 2A, 2B and Familial Medullary Thyroid Cancer: RET
- Peutz-Jeghers Syndrome: STK11
- Juvenile Polyposis: BMPR1A, SMAD4
- Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC): FH
- Birt-Hogge-Dubé Syndrome: FLCN
- Hereditary Melanoma: CDKN2A, CDK4
- Von Hippel-Lindau Syndrome: VHL
- Neurofibromatosis: NF1
- DICER1 Syndrome: DICER1
- BAP1 Syndrome: BAP1
To learn more about genomic testing, contact the Center for Cancer Genetic and Prevention at Dana-Farber/Brigham and Women’s Cancer Center.