| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ARID1B, LOC115308161
+1 more (S136L) | Single nucleotide variant (missense variant) | not provided | GConflicting classifications of pathogenicity |
| | ARID1B, LOC115308161
+1 more | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | |
| | ARID1B, LOC115308161
+1 more (A141T +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | ARID1B, LOC115308161
+1 more (N66S +1 more) | Single nucleotide variant (missense variant) | ARID1B-related condition +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene