ابزارهای پیش بینی می توانند جهش های نادر را با جهش های خطرناک اشتباه بگیرند

Predictive tools can confuse rare mutations with dangerous ones

When a patient's DNA is read, it is compared with a reference version of the human genome. This allows geneticists and rare disease experts to look at a list of places where the patient's DNA differs. Most variations will be harmless and shared with millions of other people, but some can cause illness.