| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126806171, CAD (P859L +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Duplication (intron variant) | CAD-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | CAD-related condition +1 more | |
Click to view in NCBI Gene