| | | Single nucleotide variant (missense variant +1 more) | Foveal hypoplasia +18 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | TYR-related condition +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Tyrosinase-negative oculocutaneous albinism +5 more | |
| | | Single nucleotide variant (missense variant) | Oculocutaneous albinism +7 more | |
| | | Single nucleotide variant (missense variant) | Tyrosinase-negative oculocutaneous albinism +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Oculocutaneous albinism +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Tyrosinase-negative oculocutaneous albinism +5 more | |
| | | Single nucleotide variant (missense variant) | Oculocutaneous albinism +6 more | |
| | | Single nucleotide variant (missense variant) | TYR-related condition +7 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity; other |
| | | Single nucleotide variant (missense variant) | TYR-related condition +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Tyrosinase-negative oculocutaneous albinism +4 more | |
| | | Single nucleotide variant (missense variant) | Oculocutaneous albinism type 1B +2 more | |
| | | Single nucleotide variant (missense variant) | Tyrosinase-negative oculocutaneous albinism +5 more | |
| | | Duplication (frameshift variant) | not provided +3 more | GPathogenic/Likely pathogenic |