| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KIDINS220 (A1222T +6 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | KIDINS220 (I1026T +2 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene