| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | ARID1B, LOC129997525 (V227P +1 more) | Indel (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene