| | | Single nucleotide variant (nonsense) | HTRA1-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant) | Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | CARASIL syndrome | |
| | | Single nucleotide variant (intron variant) | CARASIL syndrome +2 more | |
| | | Single nucleotide variant (nonsense) | CARASIL syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | CARASIL syndrome | |
| | | Single nucleotide variant (nonsense) | CARASIL syndrome +1 more | GConflicting classifications of pathogenicity |
| | | | CARASIL syndrome | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | CARASIL syndrome +2 more | |
| | | Deletion (frameshift variant) | CARASIL syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | CARASIL syndrome | |
| | | Single nucleotide variant (missense variant) | HTRA1-related cerebral small vessel disease +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | CARASIL syndrome | |
| | | Single nucleotide variant (missense variant) | CARASIL syndrome | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |