LL4034-6
ACMG_Clinical significance of genetic variation
- Answer list
- LL4034-6
- Answers
- 5
Answers
| Answer | Code | Score |
|---|---|---|
| Pathogenic | LA6668-3 | |
| Likely pathogenic | LA26332-9 | |
| Uncertain significance | LA26333-7 | |
| Likely benign | LA26334-5 | |
| Benign | LA6675-8 |
Used by 1 tests
| LOINC |
|---|
| 53037-8 |