As panels of multiple genetic tests become increasingly available, cli
nicians face new challenges in helping patients understand the nature
of these tests. Diagnostic tests for conditions that inevitably lead t
o disease, ''susceptibility'' tests that reveal heightened risk of dis
ease, and tests for carrier status raise different concerns about info
rmed consent and pose different needs for counseling. Clinicians must
understand the implications of different kinds of tests, and of differ
ent arrays of tests in multiple panels, if multiplex tests are to be u
sed wisely in clinical practice.