|
Name |
Type |
Discontinued? |
|
| 1 |
VARIANT_ID |
NUMERIC |
No |
|
|
|
| The unique identifier for the variant record. |
|
|
| 2 |
LINE |
INTEGER |
No |
|
|
|
| The line number for the information associated with this record. Multiple pieces of information can be associated with this record. |
|
|
| 3 |
PGX_MED_CODESET_C_NAME |
VARCHAR |
No |
|
|
|
| The medication coding system category for the pharmacogenomic variant. |
| May contain organization-specific values: No |
| Category Entries: |
| RxT-Ingrd |
| ATC |
|
|
| 4 |
PGX_MED_CODE |
VARCHAR |
No |
|
|
|
| Code for the medication being assessed for usage suggestions based on drug-gene interactions. |
|
|
| 5 |
ASSOC_MED_NAME |
VARCHAR |
No |
|
|
|
| Name of the medication being assessed for usage suggestions based on drug-gene interactions. |
|
|
| 6 |
MED_USE_CATEGORY_C_NAME |
VARCHAR |
No |
|
|
|
| The medication usage suggestion category for the pharmacogenomic variant. |
| May contain organization-specific values: No |
| Category Entries: |
| Consider alternative medication |
| Decrease dose |
| Increase dose |
| Use caution |
| Normal response expected |
|
|
