| Disease Name | phenotype | Inheritance Mode | Chr Location | Mutation Type | Gene Name | mRNA Variant | Protein Variant | Effect | Reference |
| Split Hand/Foot Malformation Type 6 | Typical SHFM | Autosomal Recessive | 12q13.12 | Missense | WNT10B | 986C>G | Thr329Arg | Amino Acid Substitution | 0/Khan et al., 2012 |
| Split Hand/Foot Malformation Type 6 (WNT10B) | split hands & feet | Autosomal Recessive | 12q13.12 | Missense | WNT10B | 986C>G | Thr329Arg | Amino Acid Substitution | 0/Khan et al., 2012 |
| Split Hand/Foot Malformation Type 6 (WNT10B) | split hands & feet | Autosomal Recessive | 12q13.12 | Deletion | WNT10B | 1165_1168delAAGT | Frame shift mutation & PTC | 0/Aziz et al., 2014 | |
| Split Hand/Foot Malformation Type 6 (WNT10B) | split hands & feet | Autosomal Recessive | 12q13.12 | Duplication | WNT10B | 300_306dupAGGGCGG | Frame shift mutation & PTC | 0/Aziz et al., 2014 | |
| Split Hand/Foot Malformation Type 6 (WNT10B) | Split-hand/split-foot | Autosomal Recessive | 12p11.1?q13.13 | Nonsense | WNT10B | 460C>G | Gln154* | PTC | 0/Ullah et al., 2018 |
| Split Hand/Foot Malformation Type 6 (WNT10B) | Split-hand/foot malformation 6 | Autosomal Recessive | 12q13.12 | Substitution | WNT10B | c.338G>C | p.(Gly113Ala) | Missense | Bilal et al., 2023/2023 |
| Split Hand/Foot Malformation Type 6 (WNT10B) | Split-hand/foot malformation 6 | Autosomal Recessive | 12q13.12 | Deletion | WNT10B | c.884-896delTCCAGCCCCGTCT | p.(Phe295Cysfs*87) | Frameshift | Bilal et al., 2023/2023 |
