| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +1 more | |
| | RNF213, RNF213-AS1 (T4114I) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | RNF213, RNF213-AS1 (D4122A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene