| Disease Name | phenotype | Inheritance Mode | Chr Location | Mutation Type | Gene Name | mRNA Variant | Protein Variant | Effect | Reference |
| Nonhemolytic U H (UGT1A1) | nonhemolytic U.H | Autosomal Recessive | 2q37.1 | Missense | UGT1A1 | 689A>G | Tyr230Cys | Amino Acid Substitution | Khan et al., 2013/2013 |
| Nonhemolytic U H (UGT1A1) | nonhemolytic U.H | Autosomal Recessive | 2q37.1 | Missense | UGT1A1 | 106G>A | Asp36Asn | Amino Acid Substitution | Khan et al., 2013/2013 |
| Nonhemolytic U H (UGT1A1) | nonhemolytic U.H | Autosomal Recessive | 2q37.1 | Duplication | UGT1A1 | 622-625dupCAGC | Ser208fs*258 | Frame shift mutation & PTC | Khan et al., 2013/2013 |
| Nonhemolytic U H (UGT1A1) | nonhemolytic U.H | Autosomal Recessive | 2q37.1 | Nonsense | UGT1A1 | 1021C >T | Arg341* | Premature Termination | Khan et al., 2013/2013 |
| Nonhemolytic U H (UGT1A1) | nonhemolytic U.H | Autosomal Recessive | 2q37.1 | UGT1A1 | A(TA)7TAA | Khan et al., 2013/2013 |
