Ensure the patients’ understanding of the given genetic information |
6.53 |
0.96 |
Draw Pedigree |
6.50 |
0.99 |
Collect information for genetic investigation |
6.47 |
0.88 |
Help patients express their own questions |
6.46 |
0.91 |
Inform the patient about prenatal testing |
6.34 |
1.14 |
Make genetic risk assessment |
6.32 |
1.06 |
Inform the patient about diagnostic testing |
6.27 |
1.24 |
Inform the patient about reproductive options |
6.24 |
1.24 |
Inform the patient about presymptomatic testing |
6.23 |
1.26 |
Inform the patient about test result |
6.16 |
1.47 |
Guide the patient in making the right decision for themselves |
6.05 |
1.38 |
Inform the patients about familial risk (without known mutation) |
5.99 |
1.27 |
Give the patient clinical and medical information |
5.99 |
1.44 |
Discuss with the patient the potential effect on every-day life |
5.80 |
1.5 |
Coordinate the care pathway with other health care practitioners as well |
5.78 |
1.53 |
Provide psychological support to the patient |
5.77 |
1.4 |
Identify and help patients in crisis |
5.70 |
1.47 |
Provide follow-up after a clinical visit |
5.65 |
1.53 |
Literature research |
5.64 |
1.59 |
Discuss common psychological reactions and feelings |
5.59 |
1.35 |
Education of the population |
5.45 |
1.52 |
Inform the patient about genetic variants of unclear significance |
5.43 |
1.68 |
Make a diagnosis |
5.15 |
2.04 |
Write referrals |
5.11 |
1.7 |
Sample handling |
5.04 |
1.74 |