| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | not provided +1 more | |
| | | Microsatellite (splice donor variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Primary hyperoxaluria, type II +2 more | |
| | | Microsatellite (intron variant) | not specified +1 more | |
Click to view in NCBI Gene