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Despite displaying symptoms of lactose intolerance, my report shows low risk for it. Why?

The information contained in the report is curated from peer-reviewed studies, and based on the number of risk variants present in your DNA raw data file, the genetic risk of a particular condition is indicated as likely low, medium, or high. For lactose intolerance, we analyze the variants of LCT and MCM6 genes. People carrying a specific variant of these genes may tend to display the symptoms of lactose intolerance. However, the symptoms can be triggered by other factors like irritable bowel syndrome, lesser-known genetic factors or it could be a reaction to casein in milk.
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