| | | Single nucleotide variant (synonymous variant +1 more) | Huntington disease-like 1 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Fatal familial insomnia +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Spongiform encephalopathy with neuropsychiatric features | |
| | | Single nucleotide variant (synonymous variant +1 more) | Spongiform encephalopathy with neuropsychiatric features | |
| | | Single nucleotide variant (3 prime UTR variant) | Inherited prion disease +7 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +7 more | |
| | | Microsatellite (inframe_deletion) | Spongiform encephalopathy with neuropsychiatric features +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Spongiform encephalopathy with neuropsychiatric features | |
| | | Single nucleotide variant (missense variant +1 more) | Spongiform encephalopathy with neuropsychiatric features +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Huntington disease-like 1 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Huntington disease-like 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Huntington disease-like 1 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Gerstmann-Straussler-Scheinker syndrome +6 more | GPathogenic/Likely pathogenic/Pathogenic, low penetrance |
| | | Single nucleotide variant (missense variant +1 more) | Fatal familial insomnia +6 more | GPathogenic/Likely pathogenic/Pathogenic, low penetrance |
| | | Single nucleotide variant (missense variant +1 more) | Inherited Creutzfeldt-Jakob disease +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inherited Creutzfeldt-Jakob disease +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inherited Creutzfeldt-Jakob disease +3 more | |