| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KCNK12, LOC129933697
+1 more (D358A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KCNK12, LOC129933697
+1 more (S357R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KCNK12, LOC129933697
+1 more (D356A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene