Released: 3-Feb-2015 9:00 AM EST Source Newsroom: 23andMe Contact Information Available for logged-in reporters only Newswise Mountain View, California February 3, 2015 23andMe, Inc., the leading personal genetics company, today announced the publication of the first ever genome-wide association study of motion sickness. Published in Oxford Journals Human Molecular Genetics, this study is the first to identify genetic variants associated with motion sickness, a condition that affects roughly one in three people. Motion sickness has been shown to have high heritability, meaning genetics accounts for a large part of why some are more prone to motion sickness than others. Estimates indicate that up to 70 percent of variation in risk for motion sickness is due to genetics (1). Until now theres been a poor understanding of the genetics of motion sickness, despite it being a fairly common condition, said 23andMe Scientist Bethann Hromatka, lead author of the study. With the help of 23andMe customers weve been able to uncover some of the underlying genetics of this condition. These findings could help provide clues about the causes of motion sickness and other related conditions, and how to treat them, which is very exciting. The study, which involved the consented participation of … Continue reading
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