The focus of clinical genetics, and thus genetic counselling, is forecast t
o expand from the diagnosis and prediction of rare, often untreatable condi
tions, to the prediction of common, often treatable or preventable conditio
ns'. Whether this evolution is likely to proceed rapidly or at a pace that
permits sensible integration of molecular genetic tools is unknown and a so
urce of debate(2,3) . It is clear, however, that genetic discoveries will m
odify the way in which disease and risk are conceptualized. Here, we predic
t how genetic counselling, specifically for more common diseases, might be
provided in the decades to come. We envisage an expansion of professional r
oles and expertise for many health care providers and highlight the need fo
r counselling practices to become more evidence based. Although we support
an evidentiary-based approach to the integration of genetic testing into pr
actice, genetic advance is unlikely to occur in an orderly and standardized
manner within countries, much less among different countries and health ca
re systems(4). Geneticists will become increasingly involved in professiona
l education and policy-making regarding genetic testing and screening progr
ams.