A population of about 5 million at the northern corner of Europe is unlikel
y to arouse the attention of the human genetics community, unless it offers
something useful for others to learn. A combination of coincidences has fi
nally made this population one that, out of proportion for its size, has by
example shaped research in human disease genetics. This chapter summarizes
advances made in medical genetics that are based on research facilitated b
y Finland's population structure. The annotation of the human genome for it
s polymorphism and involvement in disease is not over; it is, therefore, of
interest to assess whether genetic studies in populations such as the Finn
ish might help in the remaining tasks.