Links from MedGen
Items: 3
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KRT18, LOC106096416 (E200G) | Single nucleotide variant (missense variant) | Cirrhosis, familial | |
| | KRT18, LOC106096416 (D181N) | Single nucleotide variant (missense variant) | Cirrhosis, familial | |
| | LOC106096416, KRT18
+1 more (G69A) | Single nucleotide variant (missense variant +1 more) | Cirrhosis, familial +1 more | |
Click to view in NCBI Gene