Jan 10
The past year in genetics has held no shortage of surprises. Fossilized bone fragments helped to rewrite parts of the Neanderthal story, including how some bands migrated and lived. A team of researchers in Spain learned the dopplegängers have more in common than meets the eye. The phrase “superdodger: officially entered COVID-19 lexicon. A...
Dec 9
Not too long ago, 23andMe launched a new study of sarcoidosis, specifically aimed at better understanding the underlying genetic and environmental factors that contribute to sarcoidosis in individuals with African ancestry. Sarcoidosis (pronounced SAR-COY-DOE-SIS) is a rare inflammatory disease that affects the Black community at double the...
Nov 10
In the latest update to 23andMe’s Ancestry Reports and features, we’ve added finer detail for customers with Ashkenazi Jewish ancestry allowing them to trace their family connections back to seven genetic groups corresponding to regions within Eastern and Central Europe. Some of these regions overlap, but they map to areas with deep his...
Oct 11
After your 23andMe reports comes back, you might have questions about what to do next. When the question around a DNA result revolves around genetics and your health, that’s where a healthcare provider fits in. 23andMe reports can provide you with powerful information about health predispositions, pharmacogenetics, wellness, and more. Let...
Sep 20
23andMe released a new report (powered by 23andMe Research) on Fibromyalgia for 23andMe+ members. Fibromyalgia is characterized by chronic pain and tenderness throughout the body. That pain can be intermittent and move to different parts of the body. Fibromyalgia symptoms can also include fatigue, problems sleeping, and difficulty concentratin...
Sep 8
Listening to those with a rare disease, a common refrain is that they often feel isolated, unheard, and alone. But, they’re not alone, 23andMe says. Much to Learn While each rare disease is by definition uncommon - affecting fewer than 200,000 people - there are more than 7,000 known rare diseases. There are more than 300 million peopl...
Aug 25
23andMe announced that a new genetic study identified five regions in the human genome associated with susceptibility to pneumonia, a leading cause of death worldwide. Published in the journal Nature Communications, the study also found a surprising link between the risk of pneumonia and psychiatric conditions, such as schizophrenia, bipola...
Jul 13
23andMe released a new report Powered by 23andMe Research on Rosacea for 23andMe+ members. Rosacea is a chronic skin condition that typically affects the central parts of the face. It is commonly characterized by flushing, redness, and visible blood vessels, but symptoms can vary; some individuals experience irritation or inflammation of th...
Jun 21
23andMe updated its report on an inherited condition characterized by mild to profound hearing loss. The update to 23andMe’s Nonsyndomic Hearing Loss and Deafness, DFNB1 (GJB1-Related) Carrier Status Report adds six variants that improve the coverage of the test for people with East Asian, Southeast Asian, and South Asian ancestry. “We ...
Jun 1
In what is among the largest studies of long COVID to date, researchers at 23andMe confirm that it disproportionately impacts women, and being diagnosed with depression or anxiety is associated with more than a two-fold increase in risk for the condition. The study also found that about half of those with persistent symptoms are experiencing ...