| | | 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 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859685, TNFRSF21 (P242R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859685, TNFRSF21 (R232C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859685, TNFRSF21 (R173W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859685, TNFRSF21 (V152L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859685, TNFRSF21 (V149A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859685, TNFRSF21 (M117V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859685, TNFRSF21 (I103V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126859685, TNFRSF21 (P92T) | 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 | |