| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | IFT172, LOC126806173 (E1238A) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (intron variant) | Short-rib thoracic dysplasia 10 with or without polydactyly +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene