| | | Single nucleotide variant (splice acceptor variant +1 more) | Retinal dystrophy +2 more | |
| | VCAN, VCAN-AS1 (K365I +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (P1376R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (I391V +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (C409S +1 more) | Single nucleotide variant (intron variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (G426E +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (R1431C +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (T1459M +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | |
| | VCAN, VCAN-AS1 (L1461M +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (S1512C +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (K1516E +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +4 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (P1539R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (V1540A +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (S1548L +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (E1550V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (Y595C +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (S647Y +1 more) | Single nucleotide variant (missense variant +1 more) | VCAN-related condition +2 more | |
| | VCAN, VCAN-AS1 (M665V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (Q674R +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (I1669S +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (S693R +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (Y1690C +1 more) | Single nucleotide variant (missense variant +1 more) | VCAN-related condition +2 more | |
| | VCAN, VCAN-AS1 (E726Q +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (S1716C +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (Q758R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (T1787A +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (P804T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (V1792I +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (A1804T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (Q1805R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (I825V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (S843F +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +4 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (D856N +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (T861A +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (G881D +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (S1879F +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (I919V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (R1911Q +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (D1937N +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (M1955V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (I1983L +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (D1055N +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (E2043K +1 more) | Single nucleotide variant (missense variant +1 more) | Vitreoretinopathy +3 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (V1091I +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (V1093F +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN-AS1, VCAN (Q1103R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (A1108T +1 more) | Single nucleotide variant (missense variant +1 more) | VCAN-related condition +2 more | |
| | VCAN, VCAN-AS1 (E1135D +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (Y2155N +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (K1174R +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (P2217S +1 more) | Single nucleotide variant (missense variant +1 more) | Wagner syndrome +4 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (E1304V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (D1313N +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (T1358M +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (I2355V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (E2393K +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (Y2425H +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (A2446V +1 more) | Single nucleotide variant (missense variant +1 more) | Wagner syndrome +2 more | |
| | VCAN, VCAN-AS1 (S1469N +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (V2460I +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN-AS1, VCAN (A1487T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (A2476G +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (K2497E +1 more) | Single nucleotide variant (missense variant +1 more) | Vitreoretinopathy +4 more | |
| | VCAN, VCAN-AS1 (T2516I +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (G2518S +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (R1536H +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (Y1636C +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (T1669I +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (S2661N +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (T1684K +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (D2684E +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (E1718G +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (Y2751H +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (V2774A +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (A1796T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | VCAN, VCAN-AS1 (H1853R +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (P1857A +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (A1861S +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (P1863T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (V1883I +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (E1894V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (E1927K +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (T1971I +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (G1983D +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (A3035T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (T2058I +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | VCAN, VCAN-AS1 (E3064G +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (I2088F +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | VCAN, VCAN-AS1 (R1338S +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (D3122N +3 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | VCAN, VCAN-AS1 (Q1369H +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (L3204P +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | VCAN, VCAN-AS1 (I1453V +3 more) | Single nucleotide variant (missense variant) | Vitreoretinopathy +3 more | GConflicting classifications of pathogenicity |
| | VCAN-AS1, VCAN
+1 more (R1484H +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |