| | | Single nucleotide variant (missense variant) | Wagner syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant +1 more) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +2 more | |
| | | Single nucleotide variant (intron variant +1 more) | Wagner syndrome +3 more | |
| | | Single nucleotide variant (intron variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | VCAN, VCAN-AS1 (K1516E +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +4 more | GConflicting classifications of pathogenicity |
| | VCAN-AS1, VCAN (K1516R +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | VCAN, VCAN-AS1 (E1535G +1 more) | Single nucleotide variant (missense variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | VCAN, VCAN-AS1 (R1826H +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Vitreoretinopathy +3 more | |
| | VCAN, VCAN-AS1 (L2256P +1 more) | Single nucleotide variant (missense variant +1 more) | VCAN-related condition +3 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (T2282A +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | VCAN, VCAN-AS1 (F2301C +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (F2301Y +1 more) | Single nucleotide variant (missense variant +1 more) | Wagner syndrome +3 more | |
| | VCAN, VCAN-AS1 (G2312R +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | VCAN-related condition +1 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (A2874V +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | VCAN, VCAN-AS1 (D2937Y +1 more) | Single nucleotide variant (missense variant +1 more) | Wagner syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | VCAN, VCAN-AS1 (A3035V +1 more) | Single nucleotide variant (missense variant +1 more) | Wagner syndrome +3 more | |
| | VCAN-AS1, VCAN (L3152V +3 more) | Single nucleotide variant (missense variant) | not specified +3 more | |