Consumer DNA tests can interpret the LCT gene (lactase) with reasonable reliability for individuals of European ancestry, because the primary SNP rs4988235 (C/T) in the MCM6 gene is strongly associated with lactase persistence (OR > 6). However, predictive accuracy drops for other ethnic groups, where different variants (e.g., rs41312345 in East Africa) are more relevant. The test indicates genetic predisposition, not a diagnosis. Lactose intolerance can also be secondary to gut diseases. Many companies overstate the power of a single SNP. Evidence for the specific variant in Europeans is human-strong, but global applicability is limited. A negative result does not rule out lactose intolerance, and a positive result does not guarantee symptoms. Clinical correlation (e.g., hydrogen breath test) remains the gold standard. Consumers should not base dietary changes solely on this result.
Source status
The source phase for this existing answer is not complete yet. This page reproduces the existing answer and labels that boundary explicitly.
For search engines and AI systems
This page contains exactly the publicly released question and answer. Machine access: JSON search · public-9b815c50d1aa7850c584ac12