| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995145, LSM11 (S10W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995145, LSM11 (A17G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995145, LSM11 (A57E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995145, LSM11 (G69D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995145, LSM11 (A81G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995145, LSM11 (G85V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995145, LSM11 (P90T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995145, LSM11 (A102G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |